- Basic information
- CohesinDB ID: CDBP00419385
- Locus: chr21-39060621-39063414
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Data sourse: ENCSR000BLD, GSE72082, GSE116868, GSE105028, GSE25021, GSE131606, ENCSR000EDW, GSE143937, GSE67783, ENCSR000BKV, GSE86191, GSE76893, GSE206145-NatGen2015, GSE120943, ENCSR703TNG, ENCSR000EEG, GSE98367, ENCSR000BLS, GSE206145, ENCSR000BTQ, ENCSR167MTG, GSE111913, ENCSR054FKH, ENCSR153HNT, GSE68388
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Cell type: MCF-7, H1-hESC, Macrophage, Fibroblast, HCT-116, Monocytes, Hep-G2, MB157, RPE, DKO, RT-112, K-562, HSPC, HuCC-T1, H9-hESC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 10% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.833
- Subunit: SA1,Rad21,SMC1,SA2,SMC3
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CTCF binding site: 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: False
ChIA-PET loops: True
- Compartment:
96% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"15_Quies": 54%,
"14_ReprPCWk": 18%,
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, XBP1, SUZ12, PBX2, ATF3, RUNX3, ZSCAN4, ZNF506, TEAD1, TRIM28, SNAI2, LMO2, ESR1, OCA2, CTCF, MNT, E2F4, E2F1, TFAP2C, BRD1, ZSCAN5D, MYCN, POU5F1, RUNX1T1, TOP2A, ZNF263, ZBTB48, DUX4, DDX5, ERG2, ERG, ASCL1, OGG1, MYC, SMARCA4, RAD21, GRHL3, XRCC5, NR3C1, EZH2, GRHL2, GABPB1, SPI1, SIX2, RUNX1, CTNNB1, SMC1A, CBX1, SIRT6, ZFX, TET2, ERG3, ZBTB2, RUNX2, PBX4, DAXX, ATF2, PRDM9, FOS, TEAD3, SCRT2, BCL11A, GSPT2, IKZF5, AATF, SMC3, STAG1, ZNF283, TRP47, MEF2B, TBL1X, AGO1, WT1, KDM1A, ZNF19, YY1, RELA, NEUROD1, JUNB, MCM3, SP140, BATF, MAF1, MAX, SPIB, ZNF143, PLAG1, NEUROG2, NR2F1, KDM5B, TP53, EGR2, AR, RXR, EGR1, HSF1, ZBTB26, SCRT1, BRD4, MAZ, AHR, FOSL2
- Target gene symbol (double-evidenced CRMs): ERG,ETS2
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 21
- Related genes and loops
- Related gene:
ENSG00000157554,
ENSG00000157557,
- Related loop:
chr21:38525000-38550000~~chr21:39050000-39075000,
chr21:38700000-38725000~~chr21:39050000-39075000,
chr21:38732695-38735241~~chr21:39066299-39068801,
chr21:38732707-38735284~~chr21:39066439-39068713,
chr21:38732918-38735320~~chr21:39066991-39068385,
chr21:38733115-38735333~~chr21:39066051-39068459,
chr21:38733311-38735294~~chr21:39065920-39068738,
chr21:38800000-38825000~~chr21:39050000-39075000,
chr21:38804213-38806093~~chr21:39065920-39068738,
chr21:38850000-38875000~~chr21:39050000-39075000,
chr21:38875000-38900000~~chr21:39050000-39075000,
chr21:38900000-38925000~~chr21:39050000-39075000,
chr21:38925000-38950000~~chr21:39050000-39075000,
chr21:38950000-38975000~~chr21:39050000-39075000,
chr21:38992131-38994558~~chr21:39065920-39068738,
chr21:39006962-39008700~~chr21:39066299-39068801,
chr21:39061365-39062529~~chr21:39125341-39127059,