- Basic information
- CohesinDB ID: CDBP00416979
- Locus: chr21-32472299-32473135
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Data sourse: GSE67783, ENCSR153HNT, GSE86191
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Cell type: K-562, HCT-116, HSPC
- 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: Intragenic
- 3D genome
- TAD boundary: non-Boundary
- Chromatin hubs: Hub
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Hi-C loops: True
Hi-ChIP loops: False
ChIA-PET loops: True
- Compartment:
90% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"5_TxWk": 40%,
"15_Quies": 32%,
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, PGR, XBP1, FOXA1, MLL4, ZFHX2, TFAP4, ATF3, HNRNPUL1, THAP1, PRDM1, TP63, CDC5L, CDX2, TEAD1, ELF1, RBM39, ETV1, KLF6, ESR1, USF2, CTCF, TCF12, JUN, BAF155, EP300, E4F1, MNT, TRIM24, SMC1, TFAP2C, EED, POU2F2, CHD8, NANOG, ZNF263, MYCN, TOP2A, ID3, POU5F1, ZMYND11, MTA2, ZBTB48, ZSCAN5A, STAT1, ERF, ERG2, TBP, HNF4G, ERG, HOXC5, PBX1, ASCL1, MYC, ONECUT1, SMARCA4, RAD21, FOXP2, RXRA, GABPA, STAT3, UBN1, NKX3-1, IKZF1, RCOR1, DNMT3B, DACH1, ZNF750, NR3C1, CEBPB, ESRRA, CREB1, EZH2, GRHL2, FEZF1, ZNF652, EBF3, TRPS1, ZKSCAN5, EHF, IRF1, HDAC2, GATA2, SSRP1, ZSCAN29, FLI1, MXI1, SMARCA5, RELB, NCOA2, RUNX1, AFF4, ZFX, SIN3A, SMAD3, ZNF770, CBX8, ERG3, ZNF513, SMARCC1, CREBBP, ZNF384, RUNX2, GATA4, NRF1, ARNT, PBX4, DAXX, PBX3, CDK8, SNRNP70, MED1, ZMYM3, PIAS1, NR1H2, ZNF22, BCL11A, SP1, NIPBL, HNF4A, ARID2, ARID1A, ZNF479, RBM25, ATF7, ASH2L, HNRNPLL, PHIP, BCOR, FOXP1, TCF3, ZNF623, SMC3, STAG1, MLLT1, CBFA2T2, ZNF316, TBL1X, FOXA2, PPARG, EBF1, SS18, PAF1, WT1, ZBTB33, HOXB13, KDM1A, YY1, RELA, JUNB, NEUROD1, BRG1, SP140, ZFP36, HIF1A, GATA3, TAL1, MAX, GATA1, CBX2, TLE3, KLF4, NCOA3, NR2F2, NR2F1, TCF7L2, KDM5B, TP53, EGR2, ELF3, AR, ZBTB40, RXR, EGLN2, ZNF366, EGR1, HSF1, RNF2, NCOR1, BRD4, JUND, MAZ, AHR, FOSL2
- Target gene symbol (double-evidenced CRMs): CFAP298-TCP10L,IL10RB,EVA1C,AP000295.1,URB1,CFAP298
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 45
- Number of somatic mutations (non-coding): 14
- Related genes and loops
- Related gene:
ENSG00000142207,
ENSG00000166979,
ENSG00000265590,
ENSG00000159079,
ENSG00000249624,
ENSG00000243646,
- Related loop:
chr21:31275000-31300000~~chr21:32475000-32500000,
chr21:32025000-32050000~~chr21:32450000-32475000,
chr21:32300000-32325000~~chr21:32450000-32475000,
chr21:32450000-32475000~~chr21:32575000-32600000,
chr21:32450000-32475000~~chr21:33275000-33300000,
chr21:32475000-32500000~~chr21:32575000-32600000,