- Basic information
- CohesinDB ID: CDBP00419583
- Locus: chr21-39704596-39707757
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Data sourse: GSE206145-GSE177045, GSE104888, GSE72082, ENCSR000BSB, ENCSR501LQA, ENCSR760NPX, ENCSR000BLY, ENCSR150EFU, GSE105028, GSE121355, GSE103477, GSE131606, ENCSR330ELC, GSE25021, ENCSR000BUC, GSE115602, ENCSR000EFJ, ENCSR000BTU, GSE93080, GSE67783, GSE86191, GSE138405, GSE76893, GSE101921, GSE135093, GSE51234, GSE206145-NatGen2015, GSE138105, ENCSR703TNG, ENCSR199XBQ, GSE116344, GSE94872, ENCSR895JMI, ENCSR193NSH, ENCSR768DOX, ENCSR000EHW, GSE206145, ENCSR981FDC, ENCSR247LSH, ENCSR807WAC, ENCSR000EHX, ENCSR620NWG, ENCSR767DFK, ENCSR495WGO, ENCSR984DZW, GSE97394, ENCSR217ELF, ENCSR000BTQ, ENCSR853VWZ, ENCSR956LGB, ENCSR944ZCT, GSE110061, GSE129526, ENCSR000HPG, ENCSR676MJK, ENCSR335RKQ, GSE126990, GSE50893, ENCSR748MVX, GSE64758
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Cell type: MDM, RH4, GM2610, SLK, GP5d, H9-hESC, RPE, Fibroblast, Ishikawa, GM2255, IMR-90, DKO, H1-hESC, GM12878, GM2588, SK-N-SH, HUES64, MCF-7, Hela-Kyoto, HCT-116, MCF-10A, A-549, HUVEC, HSPC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 28% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.733
- Subunit: NIPBL,SA1,Rad21,SMC1,SA2,Mau2,SMC3
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CTCF binding site: CTCF
CTCF motif: False
- Genomic location: Intragenic
- 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:
"15_Quies": 42%,
"14_ReprPCWk": 20%,
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: CBX1, SMC1A, FOXA2, EBF1, SIN3A, STAG2, FOXA1, CDK9, RELA, RAD21, NKX2-1, GATA3, TAL1, CEBPB, TEAD1, EZH2, ESR1, GRHL2, EBF3, CTCF, SMC1, SMC3, STAG1
- Target gene symbol (double-evidenced CRMs): SH3BGR,GET1-SH3BGR,GET1,BRWD1,PSMG1,B3GALT5,LCA5L,MX1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000183527,
ENSG00000185658,
ENSG00000285815,
ENSG00000182093,
ENSG00000157578,
ENSG00000185437,
ENSG00000183778,
ENSG00000157601,
- Related loop:
chr21:39100000-39125000~~chr21:39700000-39725000,
chr21:39150000-39175000~~chr21:39700000-39725000,
chr21:39225000-39250000~~chr21:39700000-39725000,
chr21:39300000-39325000~~chr21:39700000-39725000,
chr21:39400000-39425000~~chr21:39700000-39725000,
chr21:39500000-39525000~~chr21:39675000-39700000,
chr21:39500000-39525000~~chr21:39700000-39725000,
chr21:39517168-39519542~~chr21:39705393-39707110,
chr21:39517303-39519751~~chr21:39705185-39706929,
chr21:39517303-39519751~~chr21:39712480-39713816,
chr21:39517354-39519438~~chr21:39705387-39706980,
chr21:39517354-39519438~~chr21:39712470-39713909,
chr21:39517358-39519642~~chr21:39705371-39706965,
chr21:39517360-39519534~~chr21:39705354-39706952,
chr21:39517360-39519534~~chr21:39712511-39713822,
chr21:39517407-39519894~~chr21:39705344-39706807,
chr21:39517544-39519746~~chr21:39705156-39706958,
chr21:39525000-39550000~~chr21:39700000-39725000,
chr21:39550000-39575000~~chr21:39700000-39725000,
chr21:39600000-39625000~~chr21:39700000-39725000,
chr21:39700000-39725000~~chr21:41425000-41450000,