- Basic information
- CohesinDB ID: CDBP00419411
- Locus: chr21-39159537-39161498
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Data sourse: GSE118494, GSE206145-GSE177045, GSE67783, GSE86191, GSE206145, ENCSR153HNT, GSE25021, GSE50893, GSE73207
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Cell type: MCF-7, RPE, HCT-116, Hep-G2, TF-1, IMR-90, K-562, GM19239, HSPC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 2% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.900
- Subunit: SA1,Rad21,SMC1,SA2,Mau2,SMC3
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CTCF binding site: CTCF
CTCF motif: True
- Genomic location: Intergenic
- 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:
96% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): False
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Chromatin annotation:
"15_Quies": 70%,
"7_Enh": 14%,
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: PGR, NME2, XBP1, FOXA1, PBX2, ATF3, THAP1, JMJD1C, TRIM28, LMO2, ESR1, OCA2, USF2, CTCF, GATA6, SOX4, IRF4, ZNF528, TEAD4, RBPJ, TFAP2C, POU2F2, CHD8, ZSCAN5D, ZNF263, MYCN, TOP2A, RUNX1T1, POU5F1, KDM4C, CTBP1, ZBTB48, SAP130, ERG, ASCL1, MYC, EZH1, ARID1B, RAD21, GRHL3, XRCC5, ZNF614, IKZF1, RCOR1, NR3C1, CEBPB, CREB1, GRHL2, EBF3, SPI1, MIXL1, IRF1, GATA2, ZNF644, MXD3, HCFC1R1, NCOA2, ETV5, RUNX1, SMC1A, BCL6, CEBPA, SIRT6, ZFX, TET2, CREBBP, GATA4, ZNF48, SMAD4, CDK8, MED1, TEAD3, ZNF680, C11orf30, L3MBTL2, TBX5, SETDB1, STAT5A, MAFK, BCL11A, HNF4A, NKX2-5, FOXP1, AATF, SMC3, STAG1, TRP47, CBFA2T2, AGO1, FOXA2, ZSCAN16, MAFF, WT1, FOXF1, ZNF580, YY1, RELA, NEUROD1, AHR, SP140, TCF4, OTX2, GATA3, TAL1, MAX, NRIP1, GATA1, PLAG1, NCOA3, NR2F2, NEUROG2, TCF7L2, NR2F1, ZNF334, MYOD1, ELF3, AR, HSF1, ZBTB26, NOTCH3, BRD4, JUND, RNF2, CLOCK, MAZ, ZNF316
- Target gene symbol (double-evidenced CRMs): ERG,GET1-SH3BGR,GET1,KCNJ6
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 18
- Related genes and loops
- Related gene:
ENSG00000157542,
ENSG00000157554,
ENSG00000285815,
ENSG00000182093,
- Related loop:
chr21:37675000-37700000~~chr21:39150000-39175000,
chr21:37700000-37725000~~chr21:39150000-39175000,
chr21:38150000-38175000~~chr21:39150000-39175000,
chr21:38350000-38375000~~chr21:39150000-39175000,
chr21:38375000-38400000~~chr21:39150000-39175000,
chr21:38379946-38381381~~chr21:39152646-39154555,
chr21:38475000-38500000~~chr21:39150000-39175000,
chr21:38500000-38525000~~chr21:39150000-39175000,
chr21:38525000-38550000~~chr21:39150000-39175000,
chr21:38650000-38675000~~chr21:39150000-39175000,
chr21:38700000-38725000~~chr21:39150000-39175000,
chr21:38725000-38750000~~chr21:39150000-39175000,
chr21:38850000-38875000~~chr21:39150000-39175000,
chr21:38875000-38900000~~chr21:39150000-39175000,
chr21:39000000-39025000~~chr21:39150000-39175000,
chr21:39150000-39175000~~chr21:39375000-39400000,
chr21:39150000-39175000~~chr21:39700000-39725000,
chr21:39152734-39154644~~chr21:39445170-39446634,