- Basic information
- CohesinDB ID: CDBP00415421
- Locus: chr21-26146681-26147011
-
Data sourse: GSE206145-GSE177045
-
Cell type: MCF-7
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 0% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.989
- Subunit: Mau2
-
CTCF binding site: non-CTCF
CTCF motif: False
- Genomic location: Intragenic
- 3D genome
- TAD boundary: Boundary
- Chromatin hubs: Hub
-
Hi-C loops: True
Hi-ChIP loops: False
ChIA-PET loops: True
- Compartment:
68% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
-
Chromatin annotation:
"5_TxWk": 72%,
"15_Quies": 17%,
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: FOXO1, PGR, SOX2, XBP1, FOXA1, TFAP4, ATF3, CHD7, MZF1, MITF, ZNF467, JMJD1C, TEAD1, ETV1, KLF6, SAP30, ESR1, HNF1B, OCA2, PITX3, LMO2, JUN, TCF12, BAF155, EP300, LMO1, GATA6, DPF2, E2F1, TEAD4, FOXA3, TFAP2C, EED, GLIS1, NANOG, CHD8, POU2F2, TOP2A, CDK7, RUNX1T1, DUX4, STAT1, ERG, ASCL1, ETS1, MYC, ONECUT1, EOMES, SMARCA4, RAD21, GRHL3, PROX1, NKX2-1, RXRA, GABPA, STAT3, RCOR1, NR2F6, VDR, ARNTL, NR3C1, ESRRA, CEBPB, KMT2A, BMPR1A, GRHL2, TRPS1, ZHX2, SPI1, MIXL1, EHF, IRF1, KLF17, HDAC2, GATA2, FLI1, MRTFB, RUNX1, SMC1A, CEBPA, SIN3A, ZFX, ZNF534, SMAD3, ERG3, SMARCC1, PRDM10, CREBBP, NOTCH1, RUNX2, CDK6, GATA4, ZNF184, ARNT, PBX4, SOX11, HMGB2, ATF2, FOXM1, CHD1, CDK8, FOS, MED1, ZEB1, TEAD3, MYB, SCRT2, TBX5, RBM22, BCL11A, NR4A1, REST, ARID1A, ZNF479, ASH2L, HNRNPLL, PHIP, TCF3, FOXP1, PRDM6, ELL2, NCOR2, FOXA2, RBBP5, EBF1, PAF1, CDK9, HOXB13, KDM1A, YY1, RELA, NEUROD1, JUNB, ISL1, HIF1A, OTX2, GATA3, TAL1, MAX, NRIP1, ZNF143, HAND2, KLF4, NCOA3, NR2F2, TCF7L2, KDM5B, TP53, NFKB1, MYOD1, PHOX2B, ELF3, BRD2, AR, PAX3-FOXO1, YAP1, RXR, EGLN2, NOTCH3, SCRT1, BRD4, JUND, AHR, FOSL2
- Target gene symbol (double-evidenced CRMs): APP
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000142192,
- Related loop:
chr21:24925000-24950000~~chr21:26150000-26175000,
chr21:25325000-25350000~~chr21:26125000-26150000,
chr21:25350000-25375000~~chr21:26150000-26175000,
chr21:25400000-25425000~~chr21:26150000-26175000,
chr21:25575000-25600000~~chr21:26150000-26175000,
chr21:25600000-25625000~~chr21:26150000-26175000,
chr21:25625000-25650000~~chr21:26150000-26175000,
chr21:25750000-25775000~~chr21:26150000-26175000,
chr21:25775000-25800000~~chr21:26150000-26175000,
chr21:25875000-25900000~~chr21:26150000-26175000,
chr21:25925000-25950000~~chr21:26150000-26175000,
chr21:25950000-25975000~~chr21:26125000-26150000,
chr21:25950000-25975000~~chr21:26150000-26175000,
chr21:25975000-26000000~~chr21:26150000-26175000,
chr21:26025000-26050000~~chr21:26125000-26150000,
chr21:26025000-26050000~~chr21:26150000-26175000,
chr21:26050000-26075000~~chr21:26150000-26175000,
chr21:26125000-26150000~~chr21:26675000-26700000,
chr21:26150000-26175000~~chr21:26325000-26350000,
chr21:26150000-26175000~~chr21:26375000-26400000,
chr21:26150000-26175000~~chr21:26425000-26450000,
chr21:26150000-26175000~~chr21:26525000-26550000,
chr21:26150000-26175000~~chr21:26550000-26575000,
chr21:26150000-26175000~~chr21:26700000-26725000,
chr21:26150000-26175000~~chr21:26800000-26825000,
chr21:26150000-26175000~~chr21:26825000-26850000,
chr21:26150000-26175000~~chr21:27500000-27525000,