- Basic information
- CohesinDB ID: CDBP00413464
- Locus: chr21-15289229-15290867
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Data sourse: ENCSR000BLD, ENCSR167MTG, ENCSR338DUC, GSE67783, GSE72082, GSE86191, GSE111913, ENCSR000BLS, GSE105028, GSE206145-NatGen2015, ENCSR000ECE, ENCSR054FKH, GSE206145, ENCSR153HNT, GSE116344, GSE131606, GSE38411
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Cell type: RPE, H1-hESC, Fibroblast, HCT-116, RH4, Hep-G2, RT-112, K-562, BCBL-1, HSPC, H9-hESC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 5% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.878
- Subunit: SA1,Rad21,SA2,SMC1
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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: False
ChIA-PET loops: True
- Compartment:
47% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): Enhancer
- Super enhancer (SEdb): False
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Chromatin annotation:
"15_Quies": 61%,
"7_Enh": 17%,
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, POU2F2, TBL1X, POU5F1, MYCN, ZFX, ZBTB48, WT1, YY1, RELA, OGG1, ATF3, MYC, SP140, GRHL3, CBFB, STAT3, CEBPB, HNRNPL, ESR1, CTCF, AR, HSF1, AATF, STAG1
- Target gene symbol (double-evidenced CRMs): NRIP1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 4
- Related genes and loops
- Related gene:
ENSG00000180530,
- Related loop:
chr21:14850000-14875000~~chr21:15275000-15300000,
chr21:14866344-14867733~~chr21:15291005-15294045,
chr21:14875000-14900000~~chr21:15275000-15300000,
chr21:14950000-14975000~~chr21:15275000-15300000,
chr21:15150000-15175000~~chr21:15275000-15300000,
chr21:15275000-15300000~~chr21:15375000-15400000,
chr21:15275000-15300000~~chr21:15400000-15425000,
chr21:15275000-15300000~~chr21:15425000-15450000,
chr21:15275000-15300000~~chr21:15450000-15475000,
chr21:15275000-15300000~~chr21:15475000-15500000,