- Basic information
- CohesinDB ID: CDBP00420370
- Locus: chr21-42488988-42489705
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Data sourse: GSE67783, GSE86191, GSE98367, GSE120943, ENCSR153HNT
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Cell type: HCT-116, Monocytes, K-562, HSPC, Macrophage
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 1% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.944
- Subunit: SA1,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:
88% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"14_ReprPCWk": 44%,
"15_Quies": 38%,
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: BCL6, ZNF707, ZNF621, ZFX, MTA2, STAT1, NONO, ZNF473, ZBTB33, SUZ12, DDX5, ZNF662, ZKSCAN1, HDGF, EHMT2, BRD9, ZNF148, NFIB, ZNF444, ZNF311, HMBOX1, STAT3, ZNF449, ZNF544, STAG1, NCOA1, CTCF, TCF12, MAFK, HSF1, ZNF776, MAZ, BRCA1, MLLT1
- Target gene symbol (double-evidenced CRMs): BACE2,SLC37A1,C2CD2,RSPH1,PRDM15,UMODL1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 6
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000182240,
ENSG00000141956,
ENSG00000157617,
ENSG00000177398,
ENSG00000160188,
ENSG00000160190,
- Related loop:
chr21:41200000-41225000~~chr21:42475000-42500000,
chr21:41650000-41675000~~chr21:42475000-42500000,
chr21:41700000-41725000~~chr21:42475000-42500000,
chr21:41800000-41825000~~chr21:42475000-42500000,
chr21:41900000-41925000~~chr21:42475000-42500000,
chr21:41950000-41975000~~chr21:42475000-42500000,
chr21:42125000-42150000~~chr21:42475000-42500000,
chr21:42475000-42500000~~chr21:42575000-42600000,
chr21:42475000-42500000~~chr21:43250000-43275000,
chr21:42475000-42500000~~chr21:43300000-43325000,