- Basic information
- CohesinDB ID: CDBP00415326
- Locus: chr21-25871333-25873005
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Data sourse: ENCSR000BLD, GSE104888, ENCSR230ZWH, GSE72082, ENCSR000BSB, GSE116868, ENCSR000EGW, ENCSR000BLY, GSE105028, GSE121355, GSE131606, GSE108869, GSE25021, ENCSR000BTU, GSE93080, GSE67783, ENCSR000BKV, GSE86191, GSE138405, GSE101921, GSE152721, GSE206145-NatGen2015, ENCSR703TNG, GSE106870, GSE116344, GSE145327, GSE94872, ENCSR000BLS, GSE206145, GSE85526, ENCSR000ECE, ENCSR000EHX, GSE97394, ENCSR000BTQ, ENCSR167MTG, GSE110061, GSE129526, GSE111913, ENCSR054FKH, ENCSR000EDE, GSE68388, GSE83726, GSE126990, GSE50893
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Cell type: RH4, GM2610, CVB-hiPSC, GM19240, HSPC, CVI-hiPSC, Liver, HuCC-T1, H9-hESC, RPE, Fibroblast, HEKn, Ishikawa, HeLa-S3, K-562, GM18486, GM18526, H1-hESC, SNYDER, MB157, GM12878, GM12891, GM2588, SK-N-SH, GM19239, RT-112, GM19099, HUES64, MCF-7, Hela-Kyoto, HCT-116, MCF-10A, Hep-G2, HUVEC, HCAEC, HAP1
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 16% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.600
- Subunit: SA1,Rad21,SMC1,SA2,SMC3
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CTCF binding site: CTCF
CTCF motif: True
- 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:
67% 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": 67%,
"5_TxWk": 29%,
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: POU2F2, SMC1A, CBX1, ZNF207, POU5F1, MYCN, CBX3, ZFX, POU4F2, MEIS2, XBP1, ZBTB48, TEAD4, SRF, KDM1A, YY1, RELA, ZBTB2, EHMT2, ETS1, RFX1, CTCFL, RAD21, THAP1, ARNT, GRHL3, NKX2-1, MAX, ZNF143, TEAD1, TRIM28, SNAI2, SMAD1, ESR1, OCA2, ZNF334, CTCF, ZHX2, SPI1, ZBTB7A, FLI1, MAZ, AATF, SMC1, SMC3, STAG1
- Target gene symbol (double-evidenced CRMs): GABPA,CYYR1,MRPL39,APP
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 6
- Related genes and loops
- Related gene:
ENSG00000154719,
ENSG00000154727,
ENSG00000142192,
ENSG00000166265,
- Related loop:
chr21:25600000-25625000~~chr21:25850000-25875000,
chr21:25600000-25625000~~chr21:25875000-25900000,
chr21:25606735-25609548~~chr21:25871125-25872823,
chr21:25606914-25609560~~chr21:25871146-25873235,
chr21:25750000-25775000~~chr21:25850000-25875000,
chr21:25850000-25875000~~chr21:26175000-26200000,
chr21:25850000-25875000~~chr21:26325000-26350000,
chr21:25850000-25875000~~chr21:26450000-26475000,
chr21:25850000-25875000~~chr21:26675000-26700000,
chr21:25850000-25875000~~chr21:26700000-26725000,
chr21:25871157-25873150~~chr21:26715252-26718261,
chr21:25875000-25900000~~chr21:25975000-26000000,
chr21:25875000-25900000~~chr21:26050000-26075000,
chr21:25875000-25900000~~chr21:26150000-26175000,
chr21:25875000-25900000~~chr21:26175000-26200000,
chr21:25875000-25900000~~chr21:26325000-26350000,
chr21:25875000-25900000~~chr21:26375000-26400000,
chr21:25875000-25900000~~chr21:26400000-26425000,
chr21:25875000-25900000~~chr21:26525000-26550000,
chr21:25875000-25900000~~chr21:26675000-26700000,
chr21:25875000-25900000~~chr21:26700000-26725000,
chr21:25875000-25900000~~chr21:26825000-26850000,
chr21:25875000-25900000~~chr21:28725000-28750000,