- Basic information
- CohesinDB ID: CDBP00413145
- Locus: chr21-13806228-13807204
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Data sourse: ENCSR000BLD, GSE206145-GSE177045, GSE72082, ENCSR000FAD, ENCSR501LQA, ENCSR760NPX, ENCSR000EGW, ENCSR000BLY, ENCSR150EFU, GSE103477, GSE111537, GSE131606, GSE108869, GSE25021, ENCSR000BUC, ENCSR917QNE, ENCSR000EFJ, ENCSR000BTU, GSE115602, ENCSR000EAC, GSE143937, GSE67783, ENCSR000BKV, GSE86191, GSE138405, GSE76893, GSE152721, GSE130135, ENCSR703TNG, GSE116344, ENCSR895JMI, ENCSR000EEG, GSE76815, ENCSR193NSH, ENCSR768DOX, ENCSR879KXD, ENCSR000BLS, ENCSR000EHW, GSE206145, ENCSR981FDC, ENCSR247LSH, ENCSR000BMY, ENCSR000EHX, ENCSR620NWG, ENCSR807WAC, ENCSR495WGO, ENCSR984DZW, ENCSR217ELF, ENCSR000BTQ, GSE55407, ENCSR853VWZ, ENCSR956LGB, ENCSR944ZCT, ENCSR676MJK, GSE111913, ENCSR335RKQ, ENCSR000EDE, ENCSR153HNT, GSE68388, GSE83726, GSE126990, GSE50893, ENCSR748MVX, GSE131577
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Cell type: RH4, GM2610, HSPC, Liver, HuCC-T1, GM2630, Ishikawa, GM12890, HeLa-S3, GM2255, IMR-90, K-562, GM18486, DKO, H1-hESC, SNYDER, GM12878, GM2588, SK-N-SH, GM19239, RT-112, THP-1, MCF-7, Hela-Kyoto, HCT-116, HL-60, HEK293T, Hep-G2, A-549, GM19238, OCI-AML-3, HAP1
- 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): 0.633
- Subunit: SA1,Rad21,SMC1,SA2,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: False
ChIA-PET loops: True
- Compartment:
24% 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": 79%,
"9_Het": 20%,
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: CTCF, RAD21, STAG1
- Target gene symbol (double-evidenced CRMs): RBM11,HSPA13
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 6
- Related genes and loops
- Related gene:
ENSG00000185272,
ENSG00000155304,
- Related loop:
chr21:10325000-10350000~~chr21:13800000-13825000,
chr21:10350000-10375000~~chr21:13800000-13825000,
chr21:12975000-13000000~~chr21:13800000-13825000,
chr21:13000000-13025000~~chr21:13800000-13825000,
chr21:13250000-13275000~~chr21:13800000-13825000,
chr21:13275000-13300000~~chr21:13800000-13825000,
chr21:13300000-13325000~~chr21:13800000-13825000,
chr21:13450000-13475000~~chr21:13800000-13825000,
chr21:13525000-13550000~~chr21:13800000-13825000,
chr21:13550000-13575000~~chr21:13800000-13825000,
chr21:13575000-13600000~~chr21:13800000-13825000,
chr21:13650000-13675000~~chr21:13800000-13825000,
chr21:13800000-13825000~~chr21:13950000-13975000,
chr21:13800000-13825000~~chr21:13975000-14000000,
chr21:13800000-13825000~~chr21:14025000-14050000,
chr21:13800000-13825000~~chr21:14100000-14125000,
chr21:13800000-13825000~~chr21:14125000-14150000,
chr21:13800000-13825000~~chr21:14225000-14250000,
chr21:13800000-13825000~~chr21:14375000-14400000,
chr21:13800000-13825000~~chr21:14675000-14700000,
chr21:13805524-13807565~~chr21:14118402-14121049,
chr21:13806384-13807544~~chr21:14119421-14121216,
chr21:5225000-5250000~~chr21:13800000-13825000,
chr21:6900000-6925000~~chr21:13800000-13825000,
chr21:6925000-6950000~~chr21:13800000-13825000,