- Basic information
- CohesinDB ID: CDBP00421142
- Locus: chr21-44974593-45005352
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Data sourse: ENCSR000BLD, GSE206145-GSE177045, GSE104888, ENCSR230ZWH, GSE72082, ENCSR000BSB, GSE116868, ENCSR000BLY, ENCSR404BPV, GSE105028, GSE121355, GSE131606, GSE108869, GSE25021, GSE115602, ENCSR000EFJ, ENCSR000BTU, GSE165895, GSE67783, ENCSR000BKV, GSE86191, GSE138405, GSE76893, GSE101921, GSE206145-NatGen2015, GSE120943, ENCSR198ZYJ, GSE112028, GSE130135, ENCSR703TNG, GSE106870, GSE116344, GSE145327, GSE94872, GSE118494, ENCSR000EEG, ENCSR338DUC, GSE98367, ENCSR000BLS, ENCSR000EHW, GSE85526, ENCSR000ECE, GSE206145, ENCSR000EHX, ENCSR767DFK, GSE97394, ENCSR167MTG, ENCSR853VWZ, GSE110061, GSE129526, ENCSR000HPG, GSE111913, ENCSR335RKQ, ENCSR054FKH, ENCSR000EDE, ENCSR153HNT, GSE68388, GSE83726, GSE126990, GSE50893, GSE126755, ENCSR000ECS, GSE38411
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Cell type: RH4, CVB-hiPSC, CVI-hiPSC, Liver, HuCC-T1, H9-hESC, RPE, Fibroblast, HEKn, Ishikawa, GM12890, HeLa-S3, IMR-90, BCBL-1, K-562, DKO, HFFc6, H1-hESC, Monocytes, MB157, GM12891, SK-N-SH, RT-112, HeLa-Tet-On, Macrophage, HUES64, MCF-7, GM12892, Hela-Kyoto, HCT-116, HEK293T, Hep-G2, Neurons-H1, A-549, HUVEC, HCAEC, Neutrophil, HSPC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 27% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.578
- Subunit: SA1,Rad21,SMC1,SA2,Mau2,SMC3
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CTCF binding site: CTCF
CTCF motif: True
- Genomic location: TSS,TES,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:
83% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"7_Enh": 25%,
"5_TxWk": 24%,
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: RUNX1, TRP47, ATF3, MYCN, ZHX2, NR2F1, HSF1, BRD4, ZBTB48, LEO1, AATF, ZBTB33, TP63, RBM22, AGO2, DNMT3B
- Target gene symbol (double-evidenced CRMs): ADARB1,PCBP3,COL18A1,COL6A2,POFUT2,TSPEAR,SLC19A1,PTTG1IP,FAM207A,ITGB2
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 74
- Number of somatic mutations (non-coding): 249
- Related genes and loops
- Related gene:
ENSG00000175894,
ENSG00000183255,
ENSG00000160255,
ENSG00000160256,
ENSG00000197381,
ENSG00000186866,
ENSG00000182871,
ENSG00000173638,
ENSG00000183570,
ENSG00000142173,
- Related loop:
chr21:44475000-44500000~~chr21:44975000-45000000,
chr21:44500000-44525000~~chr21:44975000-45000000,
chr21:44850000-44875000~~chr21:44950000-44975000,
chr21:44875000-44900000~~chr21:44975000-45000000,
chr21:44950000-44975000~~chr21:45075000-45100000,
chr21:44950000-44975000~~chr21:45100000-45125000,
chr21:44950000-44975000~~chr21:45125000-45150000,
chr21:44950000-44975000~~chr21:45250000-45275000,
chr21:44950000-44975000~~chr21:45275000-45300000,
chr21:44950000-44975000~~chr21:45425000-45450000,
chr21:44950000-44975000~~chr21:45450000-45475000,
chr21:44950000-44975000~~chr21:45800000-45825000,
chr21:44950000-44975000~~chr21:45825000-45850000,
chr21:44975000-45000000~~chr21:45125000-45150000,
chr21:44975000-45000000~~chr21:45200000-45225000,
chr21:44975000-45000000~~chr21:45325000-45350000,
chr21:44975000-45000000~~chr21:45425000-45450000,
chr21:44975000-45000000~~chr21:45450000-45475000,
chr21:44975000-45000000~~chr21:45500000-45525000,
chr21:44975000-45000000~~chr21:45725000-45750000,
chr21:44975000-45000000~~chr21:45800000-45825000,
chr21:44975000-45000000~~chr21:45825000-45850000,
chr21:44975000-45000000~~chr21:46100000-46125000,
chr21:45000000-45025000~~chr21:45100000-45125000,
chr21:45000000-45025000~~chr21:45125000-45150000,
chr21:45000000-45025000~~chr21:45325000-45350000,