- Basic information
- CohesinDB ID: CDBP00419539
- Locus: chr21-39573222-39573683
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Data sourse: ENCSR000BTQ, GSE206145-GSE177045, GSE72082, ENCSR000BKV, GSE98367, GSE120943, ENCSR703TNG
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Cell type: K-562, MCF-7, Monocytes, Macrophage
- 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): 0.956
- Subunit: Rad21,SMC1
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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: False
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": 46%,
"14_ReprPCWk": 35%,
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, CHD8, KDM4C, ZFX, XBP1, GTF2B, WT1, DUX4, FOXA1, ERG3, SUZ12, RELA, CREBBP, ZNF112, MYC, CTCFL, RAD21, GRHL3, NFIB, ARNT, GATA3, PRDM9, XRCC5, NRIP1, NCOA3, TEAD1, EZH2, ESR1, OCA2, GRHL2, CTCF, AR, PAX3-FOXO1, TAF1, CLOCK, MAZ
- Target gene symbol (double-evidenced CRMs): B3GALT5
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 5
- Number of somatic mutations (non-coding): 0
- Related genes and loops