- Basic information
- CohesinDB ID: CDBP00418007
- Locus: chr21-35221773-35224106
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Data sourse: ENCSR230ZWH, GSE72082, GSE98367, GSE138405, GSE129526, GSE206145, GSE101921, GSE62063, GSE206145-NatGen2015, GSE68388, ENCSR703TNG, GSE50893, ENCSR917QNE
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Cell type: GM2610, GM19240, Liver, HuCC-T1, B-cell, RPE, GM2630, Fibroblast, GM18486, GM18526, SNYDER, GM12891, GM2588, GM19239, GM19193, Macrophage, Ramos, MCF-7, GM12892, Hela-Kyoto, HCT-116, HCAEC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 8% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.756
- Subunit: NIPBL,SA1,Rad21,SMC1,SA2,Mau2,SMC3
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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: True
ChIA-PET loops: True
- Compartment:
84% 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": 33%,
"15_Quies": 30%,
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: NFIA, FOXA1, PBX2, ZFHX2, NFIC, RUNX3, ZBTB44, BACH2, MAF, JMJD1C, TEAD1, TRIM28, ELF1, KLF6, BCLAF1, ESR1, HNF1B, CTCF, JUN, BAF155, MNT, TRIM24, IRF4, ZNF776, E2F1, SMC1, TEAD4, EHMT2, RBPJ, MYCN, RUNX1T1, ID3, TOP2A, STAT1, ARID3A, ERG2, HOXC5, ERG, PBX1, MIER1, ETS1, MYC, RAD21, RXRA, GABPA, APC, STAT3, IKZF1, NR2F6, VDR, ARNTL, ESRRA, CEBPB, STAT5B, KMT2A, CREB1, GRHL2, SPI1, HDAC2, FLI1, MXI1, NR2C2, RUNX1, SMC1A, BCL6, SIN3A, SMAD3, ERG3, PRDM10, ZBTB2, RARA, ZNF384, RUNX2, PBX4, HMGB2, ETV6, FOS, MED1, MYB, SCRT2, ZMYM3, USF1, BCL11A, SP1, NR4A1, HNF4A, REST, RBM25, PHIP, TCF3, BCOR, FOXP1, AFF1, MTA3, MIER2, ESR2, MEF2C, CDK9, HOXB13, KDM1A, RELA, ZFP36, HIF1A, GATA3, TAL1, MAX, SPIB, ZNF143, NRIP1, NR2F2, NR2F1, ZNF768, KDM5B, TP53, NFKB1, EGR2, ELF3, BRD2, AR, ZBTB40, EGLN2, NCOR1, BRD4, SCRT1, ZNF24, ZNF316
- Target gene symbol (double-evidenced CRMs): SMIM11A,RUNX1,SETD4,RCAN1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000205670,
ENSG00000159200,
ENSG00000159216,
ENSG00000185917,
- Related loop:
chr21:34350000-34375000~~chr21:35200000-35225000,
chr21:34350000-34375000~~chr21:35225000-35250000,
chr21:34525000-34550000~~chr21:35200000-35225000,
chr21:34725000-34750000~~chr21:35200000-35225000,
chr21:34875000-34900000~~chr21:35200000-35225000,
chr21:34875000-34900000~~chr21:35225000-35250000,
chr21:34900000-34925000~~chr21:35200000-35225000,
chr21:34911415-34913464~~chr21:35216669-35218708,
chr21:35050000-35075000~~chr21:35200000-35225000,
chr21:35050000-35075000~~chr21:35225000-35250000,
chr21:35050055-35052229~~chr21:35226410-35228579,
chr21:35050056-35052270~~chr21:35226396-35228810,
chr21:35050107-35052241~~chr21:35221744-35223755,
chr21:35050233-35052173~~chr21:35222102-35223621,
chr21:35050370-35052249~~chr21:35226507-35228618,
chr21:35188702-35190920~~chr21:35226847-35228785,
chr21:35188826-35191178~~chr21:35226396-35228810,
chr21:35200000-35225000~~chr21:35375000-35400000,
chr21:35200000-35225000~~chr21:35400000-35425000,
chr21:35200000-35225000~~chr21:35825000-35850000,
chr21:35200000-35225000~~chr21:35925000-35950000,
chr21:35200000-35225000~~chr21:36025000-36050000,
chr21:35204264-35206999~~chr21:35221664-35223363,
chr21:35225000-35250000~~chr21:35350000-35375000,
chr21:35226847-35228785~~chr21:35339309-35341219,
chr21:35226847-35228785~~chr21:35399325-35401608,