- Basic information
- CohesinDB ID: CDBP00420089
- Locus: chr21-41645785-41646060
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Data sourse: GSE86191
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Cell type: HCT-116
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 0% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.989
- Subunit: Rad21
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CTCF binding site: CTCF
CTCF motif: False
- Genomic location: Intergenic
- 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:
89% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
-
Chromatin annotation:
"15_Quies": 48%,
"14_ReprPCWk": 28%,
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, FOSL1, PGR, HMG20A, SOX2, FOXA1, HLF, MLL4, ATF3, NFIC, ZFP64, CHD7, PRDM1, RUNX3, PAX5, TP63, MITF, MYOG, KLF5, TEAD1, ELF1, ETV1, KLF6, NFE2L2, LMO2, ESR1, TP73, JUN, TCF12, CTCF, EP300, GATA6, DPF2, SOX4, IRF4, DEK, E2F1, ZNF528, TEAD4, TFAP2C, RBPJ, EED, GLIS1, ZSCAN5D, SRC, BRD3, CDK7, TOP2A, KDM4C, MYCN, MTA2, ZBTB17, DUX4, STAT1, SRF, SAP130, NBN, HOXC5, ERG, ZNF341, ETS1, MYC, SMARCA4, EOMES, RAD21, GRHL3, RXRA, NKX2-1, STAT3, XRCC5, SOX10, UBN1, IKZF1, RCOR1, VDR, ZNF750, CEBPB, NR3C1, ESRRA, CREB1, EZH2, GRHL2, EBF3, ZHX2, SPI1, EHF, IRF1, ZNF257, GATA2, GATAD2B, SIX2, FLI1, MXI1, RELB, MRTFB, NCOA2, NFIL3, ETV5, RUNX1, SMC1A, BCL6, CEBPA, ZBTB24, SIN3A, ZFX, AFF4, SMAD3, ZNF770, ERG3, CBX8, SMARCC1, TWIST1, CREBBP, ZNF35, RARA, ZNF384, RUNX2, SMAD2, GATA4, OSR2, ZNF184, PBX4, NRF1, DAXX, ATF2, HMBOX1, SMAD4, PBX3, FOXM1, FOS, CHD1, CDK8, MED1, TEAD3, SPDEF, MYB, TBX5, MAFK, BCL11A, SP1, USF1, HNF4A, NKX2-5, REST, ATF7, ASH2L, PHIP, PRDM6, ELL2, MLLT1, MEF2B, PPARG, FOXA2, EBF1, SS18, ZNF600, ZSCAN16, MAFF, WT1, ESR2, ZBTB33, CDK9, KDM1A, YY1, RELA, TARDBP, JUNB, SP140, HIF1A, GATA3, BATF, TAL1, MAX, NRIP1, GATA1, ZNF143, CBX2, KLF4, ZNF592, SP7, NCOA3, NR2F2, TCF7L2, NR2F1, KDM5B, ZNF687, PKNOX1, TP53, SMAD1-5-8, NFKB1, MYOD1, PHOX2B, BRD2, T, ELF3, KAT8, TBX21, BHLHE40, AR, TAF1, ZBTB40, ZBTB42, HEXIM1, ZNF366, HSF1, RNF2, IKZF2, BRD4, JUND, MAZ, BRCA1, AHR, FOSL2
- Target gene symbol (double-evidenced CRMs): WDR4,HSF2BP,PRDM15,RIPK4,UMODL1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 2
- Related genes and loops
- Related gene:
ENSG00000183421,
ENSG00000141956,
ENSG00000177398,
ENSG00000160193,
ENSG00000160207,
- Related loop:
chr21:39175000-39200000~~chr21:41625000-41650000,
chr21:39625000-39650000~~chr21:41650000-41675000,
chr21:40925000-40950000~~chr21:41650000-41675000,
chr21:41625000-41650000~~chr21:41725000-41750000,
chr21:41625000-41650000~~chr21:41750000-41775000,
chr21:41625000-41650000~~chr21:41775000-41800000,
chr21:41625000-41650000~~chr21:42100000-42125000,
chr21:41625000-41650000~~chr21:42125000-42150000,
chr21:41625000-41650000~~chr21:42825000-42850000,
chr21:41625000-41650000~~chr21:43575000-43600000,
chr21:41650000-41675000~~chr21:41750000-41775000,
chr21:41650000-41675000~~chr21:41900000-41925000,
chr21:41650000-41675000~~chr21:41950000-41975000,
chr21:41650000-41675000~~chr21:42100000-42125000,
chr21:41650000-41675000~~chr21:42350000-42375000,
chr21:41650000-41675000~~chr21:42475000-42500000,
chr21:41650000-41675000~~chr21:43000000-43025000,
chr21:41650000-41675000~~chr21:43300000-43325000,
chr21:41650000-41675000~~chr21:43350000-43375000,