- Basic information
- CohesinDB ID: CDBP00417794
- Locus: chr21-34642001-34643001
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Data sourse: GSE38395, GSE93080, ENCSR000DZP, GSE206145, ENCSR000BMY, ENCSR153HNT, GSE68388, GSE50893, GSE165895
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Cell type: GM2630, GM2610, GM12878, GM2588, GM12890, hLCL, K-562, HFFc6, HuCC-T1, B-cell
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 4% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.889
- Subunit: NIPBL,SA1,Rad21,SMC1,Mau2,SMC3
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CTCF binding site: CTCF
CTCF motif: False
- Genomic location: Intergenic
- 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:
93% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): False
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Chromatin annotation:
"14_ReprPCWk": 39%,
"15_Quies": 36%,
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, XBP1, MLL4, HDGF, TSC22D4, NFIC, RUNX3, CBFB, PAX5, TP63, MITF, BACH2, JMJD1C, ELF1, BCLAF1, TEAD1, KLF6, SNAI2, ETV1, TRIM28, ZNF217, LMO2, OCA2, TP73, USF2, CTCF, TCF12, SND1, EP300, JUN, KLF1, DPF2, IRF4, ZNF350, TEAD4, RBPJ, EED, YBX1, POU2F2, ZSCAN5D, ZNF263, RUNX1T1, ID3, KDM4C, MTA2, ZSCAN5A, STAT1, NBN, ARID3A, ERG, HOXC5, PBX1, ETS1, MYC, RAD21, GRHL3, PROX1, GABPA, STAT3, IKZF1, NFE2, TERF2, NR3C1, KMT2A, ZHX2, SPI1, GATA2, GATAD2B, FLI1, SMARCA5, RELB, RUNX1, SMC1A, ZBTB24, ZFX, SMAD3, ERG3, TRIM22, MEF2A, RUNX2, ARNT, BACH1, ATF2, ETV6, PBX3, FOXM1, CDK8, SNRNP70, MED1, ZEB1, TERF1, MYB, SMAD1, EVI1, MAFK, SP1, BCL11A, NIPBL, ATF7, ASH2L, TCF3, SMC3, MLLT1, STAG1, NFATC3, MEF2B, MTA3, CREM, EBF1, HDAC6, MEIS1, GTF2B, WT1, TCF7, CDK9, BCL3, YY1, RELA, TARDBP, JUNB, SP140, TCF4, SKIL, BATF, TAL1, MAX, ZNF143, GATA1, KLF4, NCOA3, NR2F1, KDM5B, TP53, ZNF687, PKNOX1, MED, ELF3, TBX21, BHLHE40, PAX3-FOXO1, AR, TAF1, YAP1, RB1, RNF2, IKZF2, SCRT1, BRD4, NOTCH3, MAZ, AHR
- Target gene symbol (double-evidenced CRMs): MRPS6,AP000311.1,ATP5PO,SMIM11A,ITSN1,RCAN1
- Function elements
- Human SNPs: Psoriasis
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 5
- Related genes and loops
- Related gene:
ENSG00000249209,
ENSG00000205726,
ENSG00000241837,
ENSG00000243927,
ENSG00000205670,
ENSG00000159200,
- Related loop:
chr21:33900000-33925000~~chr21:34625000-34650000,
chr21:33950000-33975000~~chr21:34625000-34650000,
chr21:34125000-34150000~~chr21:34625000-34650000,
chr21:34325000-34350000~~chr21:34625000-34650000,
chr21:34350000-34375000~~chr21:34625000-34650000,
chr21:34500000-34525000~~chr21:34625000-34650000,
chr21:34625000-34650000~~chr21:35925000-35950000,
chr21:34625000-34650000~~chr21:35950000-35975000,
chr21:34640130-34641379~~chr21:34670339-34671972,
chr21:7750000-7775000~~chr21:34625000-34650000,
chr21:7800000-7825000~~chr21:34625000-34650000,