- Basic information
- CohesinDB ID: CDBP00416503
- Locus: chr21-31222011-31222540
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Data sourse: GSE152721, GSE206145-NatGen2015
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Cell type: Fibroblast, HAP1
- 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): 0.978
- Subunit: Mau2,Rad21,SA2
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CTCF binding site: non-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:
54% 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": 38%,
"5_TxWk": 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: FOSL1, PGR, HMG20A, SOX2, PATZ1, FOXA1, PBX2, MLL4, ZFHX2, HDGF, ATF3, NFIC, ZC3H8, ZNF362, ZBTB44, CHD7, IKZF3, ZNF189, PAX5, TP63, MZF1, ZNF467, ZNF629, KLF5, TEAD1, ELF1, ZNF573, KLF6, TRIM28, NFE2L2, SAP30, ESR1, OCA2, RCOR2, ZNF561, CTCF, TCF12, JUN, BAF155, KLF1, EP300, MNT, GATA6, SOX5, DPF2, E2F4, ZNF674, RAD51, E2F1, ZNF528, TEAD4, FOXA3, GATAD2A, PDX1, TFAP2C, EED, RBPJ, GLIS1, POU2F2, BRD1, ZNF263, MYCN, POU5F1, CTBP1, MTA2, ZBTB17, ZBTB48, ZSCAN5A, STAT1, NBN, ERG2, SP4, HNF4G, ERG, HOXC5, ZNF341, MYC, SMARCA4, TSHZ1, RAD21, LHX2, GRHL3, STAT3, XRCC5, SOX10, NKX3-1, PRDM14, IKZF1, RCOR1, HNRNPH1, ZNF750, CEBPB, ESRRA, NR3C1, KMT2A, CREB1, EZH2, GRHL2, FEZF1, EBF3, SPI1, EHF, KLF17, HDAC2, GATA2, GATAD2B, SIX2, FLI1, SMARCA5, RELB, RUNX1, SMC1A, CEBPA, EZH2phosphoT487, NKX2-2, SIN3A, ZFX, ZNF335, SOX13, SMAD3, ERG3, TRIM22, SMARCC1, ZNF18, CREBBP, ZNF384, ZNF35, RUNX2, GATA4, OSR2, ZNF184, PBX4, DAXX, ARNT, ATF2, ZEB2, FOXM1, MAFB, SP2, FOS, CDK8, MED1, SCRT2, SMAD1, KLF9, ZNF22, SP1, BCL11A, NIPBL, HNF4A, REST, ZBTB7A, ATF7, POU2F3, ASH2L, HOXA9, PHIP, FOXP1, PRDM6, SMC3, ELL2, NCOR2, MLLT1, NFATC3, MEF2B, PPARG, FOXA2, EBF1, MEIS1, SS18, PAF1, ZNF600, ZSCAN16, WT1, ZNF30, HOXB13, KDM1A, YY1, RELA, TARDBP, JUNB, NEUROD1, BRG1, ZIC2, HIF1A, SKIL, OTX2, GATA3, BATF, TAL1, MAX, NRIP1, ZNF143, SPIB, KLF4, CEBPG, SP7, NR2F2, TCF7L2, TP53, PKNOX1, ZBTB6, ZNF687, NFKB1, MYOD1, EGR2, PHOX2B, T, BRD2, TBX21, BHLHE40, AR, TAF1, ZBTB40, RXR, ZBTB42, EGR1, IKZF2, BRD4, SCRT1, NOTCH3, MAZ, FOSL2
- Target gene symbol (double-evidenced CRMs): TIAM1,MIS18A,HUNK
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 2
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000156299,
ENSG00000142149,
ENSG00000159055,
- Related loop:
chr21:31200000-31225000~~chr21:31300000-31325000,
chr21:31200000-31225000~~chr21:31325000-31350000,
chr21:31200000-31225000~~chr21:31375000-31400000,
chr21:31200000-31225000~~chr21:31400000-31425000,
chr21:31200000-31225000~~chr21:31425000-31450000,
chr21:31200000-31225000~~chr21:31450000-31475000,
chr21:31200000-31225000~~chr21:31550000-31575000,
chr21:31200000-31225000~~chr21:31575000-31600000,
chr21:31200000-31225000~~chr21:31600000-31625000,
chr21:31200000-31225000~~chr21:31850000-31875000,
chr21:31200000-31225000~~chr21:32250000-32275000,
chr21:31200000-31225000~~chr21:32800000-32825000,
chr21:31218191-31220098~~chr21:31343217-31344894,
chr21:31218191-31220098~~chr21:31579468-31582178,
chr21:31225000-31250000~~chr21:31325000-31350000,
chr21:31225000-31250000~~chr21:31575000-31600000,