- Basic information
- CohesinDB ID: CDBP00419923
- Locus: chr21-41179066-41179600
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Data sourse: GSE206145, GSE206145-NatGen2015, GSE72082
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Cell type: MCF-7, Fibroblast, RPE
- 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): 0.967
- Subunit: SA1,Rad21
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CTCF binding site: CTCF
CTCF motif: False
- Genomic location: TSS,TES
- 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:
67% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): False
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Chromatin annotation:
"15_Quies": 44%,
"5_TxWk": 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: PGR, POU2F2, CBFA2T2, FOXA2, MTA3, ZNF239, TOP2A, MYCN, SIRT6, ZFX, ZBTB48, PCBP2, WT1, FOXA1, ZNF770, TET2, ERG3, ERG, YY1, RELA, NOTCH1, MYC, NFIB, ZNF444, ZIC2, TAL1, NRIP1, ZNF398, TEAD1, ESR1, ZIK1, ELF3, CTCF, HES1, E4F1, GATAD2B, POU2F3, ZNF423, ZNF512B, MAZ, NCOA2, STAG1
- Target gene symbol (double-evidenced CRMs): RIPK4,FAM3B,MX1,BACE2,PRDM15
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 249
- Number of somatic mutations (non-coding): 83
- Related genes and loops
- Related gene:
ENSG00000182240,
ENSG00000183844,
ENSG00000157601,
ENSG00000183421,
ENSG00000141956,
- Related loop:
chr21:40875000-40900000~~chr21:41175000-41200000,
chr21:41075000-41100000~~chr21:41175000-41200000,
chr21:41150000-41175000~~chr21:41350000-41375000,
chr21:41150000-41175000~~chr21:41425000-41450000,
chr21:41150000-41175000~~chr21:41450000-41475000,
chr21:41150000-41175000~~chr21:41775000-41800000,
chr21:41175000-41200000~~chr21:41275000-41300000,
chr21:41175000-41200000~~chr21:41425000-41450000,
chr21:41175000-41200000~~chr21:41750000-41775000,
chr21:41175000-41200000~~chr21:41775000-41800000,