- Basic information
- CohesinDB ID: CDBP00419552
- Locus: chr21-39616321-39616816
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Data sourse: GSE206145-GSE177045
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Cell type: MCF-7
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 1% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.989
- Subunit: Mau2,Rad21
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CTCF binding site: non-CTCF
CTCF motif: False
- Genomic location: TSS
- 3D genome
- TAD boundary: Boundary
- Chromatin hubs: Hub
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Hi-C loops: True
Hi-ChIP loops: True
ChIA-PET loops: True
- Compartment:
69% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"14_ReprPCWk": 50%,
"15_Quies": 25%,
Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
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Co-bound Transcriptional factors: MBD3, FOSL1, PGR, TRIM25, ZNF660, SOX2, NME2, XBP1, PATZ1, FOXA1, SUZ12, PBX2, RING1B, ZFHX2, TFAP4, HNRNPK, MEN1, LYL1, ATF3, ZFP64, CTCFL, CHD7, IKZF3, MORC2, ZNF189, SMARCE1, TP63, ZSCAN4, MITF, ZNF320, ZNF736, HDAC3, ZNF467, ZNF629, JMJD1C, TEAD1, TRIM28, ELF1, KLF6, ETV1, KLF10, SAP30, ESR1, OCA2, ZNF217, HNF1B, LMO2, ZNF561, CTCF, JUN, TCF12, EP300, BAF155, ZBTB20, GATA6, RYBP, DPF2, E2F6, TRIM24, ZNF423, E2F1, ZNF528, TEAD4, PDX1, TFAP2C, EED, GLIS1, JARID2, NANOG, CHD8, BRD1, ZSCAN5D, MYCN, ZNF263, POU5F1, KDM4C, POU2F2, CTBP1, ZSCAN21, ZBTB17, ZBTB48, ZSCAN5A, STAT1, ZNF649, ERF, DDX5, ERG2, SP4, TBP, HOXC5, ZBTB21, ERG, ZBTB8A, ZNF341, MYC, ETS1, TSHZ1, RFX1, RAD21, KDM4A, GRHL3, GABPA, APC, STAT3, NKX3-1, ZNF398, PRDM14, RCOR1, ZNF639, NR3C1, CEBPB, ESRRA, CREB1, EZH2, KLF8, GRHL2, EBF3, TRPS1, PHF8, ZHX2, SPI1, KLF17, IRF1, ZBTB14, HDAC2, GATA2, SIX2, FLI1, MXI1, ZNF554, RUNX1, SMC1A, CBX1, EZH2phosphoT487, IRF3, SIRT6, ZNF335, ZFX, POU4F2, SIN3A, NKX2-2, SMAD3, TET2, ERG3, CBX8, SMARCC1, PRDM10, CREBBP, ZNF35, RUNX2, OSR2, ZNF184, ARNT, NRF1, PBX4, DAXX, ATF2, PRDM9, ZEB2, ZNF518A, ETV6, NCAPH2, ZNF10, FOS, CHD1, SP2, CDK8, MAFB, MED1, TEAD3, ZNF264, PIAS1, ZMYM3, TAF7, KLF9, HOXA9, STAT5A, SP1, BCL11A, TFAP2A, NIPBL, REST, ZBTB7A, RBM25, POU2F3, ASH2L, HNRNPLL, PCGF2, CTBP2, BCOR, GLIS2, FOXP1, ZNF543, PHIP, AATF, MBD2, SMC3, STAG1, TRP47, FOXA2, RBBP5, CHD2, SS18, MEIS1, ZNF600, ZNF692, ZSCAN16, WT1, GTF2B, CDK9, HOXB13, KDM1A, YY1, RELA, JUNB, BRG1, SP140, ZIC2, HIF1A, PCGF1, ZFP36, GATA3, MAF1, MAX, TAL1, NRIP1, ZNF143, MTA1, GATA1, HAND2, CBX2, TLE3, KLF4, SP7, NCOA3, NR2F2, ZNF768, TCF7L2, KDM5B, TP53, EGR2, PHOX2B, T, ELF3, BRD2, BHLHE40, AR, TAF1, ZBTB16, YAP1, ZNF324, RXR, ZNF366, ZBTB42, HEXIM1, TFIIIC, HSF1, ZBTB26, EGR1, JUND, BRD4, CLOCK, MAZ, ZSCAN23, ZNF24, AHR
- Target gene symbol (double-evidenced CRMs): SH3BGR,GET1-SH3BGR,ERG,ETS2,B3GALT5,BRWD1,PCP4,MX1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 6
- Number of somatic mutations (non-coding): 3
- Related genes and loops
- Related gene:
ENSG00000157554,
ENSG00000157557,
ENSG00000185658,
ENSG00000285815,
ENSG00000185437,
ENSG00000183778,
ENSG00000183036,
ENSG00000157601,
- Related loop:
chr21:35775000-35800000~~chr21:39600000-39625000,
chr21:38375000-38400000~~chr21:39600000-39625000,
chr21:38525000-38550000~~chr21:39600000-39625000,
chr21:38625000-38650000~~chr21:39600000-39625000,
chr21:38800000-38825000~~chr21:39600000-39625000,
chr21:38850000-38875000~~chr21:39600000-39625000,
chr21:39200000-39225000~~chr21:39600000-39625000,
chr21:39225000-39250000~~chr21:39600000-39625000,
chr21:39300000-39325000~~chr21:39600000-39625000,
chr21:39500000-39525000~~chr21:39600000-39625000,
chr21:39600000-39625000~~chr21:39700000-39725000,
chr21:39600000-39625000~~chr21:39850000-39875000,
chr21:39600000-39625000~~chr21:39900000-39925000,
chr21:39600000-39625000~~chr21:39950000-39975000,
chr21:39600000-39625000~~chr21:40050000-40075000,
chr21:39600000-39625000~~chr21:40075000-40100000,
chr21:39600000-39625000~~chr21:40100000-40125000,
chr21:39600000-39625000~~chr21:41000000-41025000,
chr21:39600000-39625000~~chr21:41075000-41100000,
chr21:39600000-39625000~~chr21:41425000-41450000,