- Basic information
- CohesinDB ID: CDBP00420513
- Locus: chr21-42867885-42870709
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Data sourse: GSE206145, GSE67783, ENCSR153HNT, GSE86191
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Cell type: K-562, HCT-116, HSPC, RPE
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 1% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.956
- Subunit: SA1,Rad21
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CTCF binding site: CTCF
CTCF motif: False
- Genomic location: Intragenic
- 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:
83% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): False
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Chromatin annotation:
"4_Tx": 64%,
"5_TxWk": 35%,
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: FOXO1, NFIA, FOSL1, ZSCAN5C, PATZ1, FOXA1, RBFOX2, LEO1, ZFHX2, HNRNPK, HDGF, ATF3, NFIC, CTCFL, CBFB, MORC2, GLYR1, ZNF189, TP63, CDX2, ELF1, RBM39, SNAI2, SMAD5, ESR1, OCA2, LMO2, USF2, CTCF, JUN, TCF12, KLF1, LMO1, GATA6, SOX4, DEK, ZNF423, GTF2F1, TFAP2C, RBPJ, JARID2, GLIS1, POU2F2, CHD8, BRD1, ZSCAN5D, MYCN, ZNF263, TOP2A, RUNX1T1, ZMYND11, ZBTB17, ZBTB48, ZSCAN5A, STAT1, DDX5, ERG2, SP4, TBP, ERG, PBX1, ASCL1, OGG1, ETS1, MYC, ONECUT1, SMARCA4, ZNF2, RAD21, GRHL3, RXRA, NKX2-1, GABPA, STAT3, APC, XRCC5, PRDM14, IKZF1, DNMT3B, HNRNPH1, NR3C1, CEBPB, SRSF3, HNRNPL, KMT2A, CREB1, KLF8, BMPR1A, EBF3, GABPB1, ZHX2, HDAC2, GATA2, MXD3, FLI1, MXI1, NCOA2, ZNF554, RUNX1, BCL6, SMC1A, CEBPA, SIRT6, CRY1, ZFX, TET2, ERG3, ZNF770, TWIST1, PRDM10, NSD2, CREBBP, ZNF35, ARNT, NFIB, ZNF48, ZNF10, SUPT5H, FOS, CHD1, SMARCB1, ZEB1, MYB, ZNF331, ZNF3, KLF9, SREBF2, ZNF22, RBM22, BCL11A, SP1, HNF4A, IKZF5, ZHX1, ASH2L, TCF3, AATF, SMC3, STAG1, TRP47, CBFA2T2, FOXA2, AGO1, PAF1, ZNF600, WT1, ZBTB33, YY1, RELA, TARDBP, NEUROD1, SP140, TCF4, HIF1A, ZIC2, KLF15, TAL1, MAX, ZNF143, AGO2, PLAG1, CBX2, KLF4, BCL11B, NR2F1, NEUROG2, KDM5B, TP53, EGR2, AR, RXR, EGLN2, HEXIM1, HSF1, ZBTB26, BRD4, MAZ, AHR
- Target gene symbol (double-evidenced CRMs): SLC37A1,WDR4,ABCG1,U2AF1,RRP1B,HSF2BP
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 14
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000160179,
ENSG00000160190,
ENSG00000160193,
ENSG00000160201,
ENSG00000160207,
ENSG00000160208,
- Related loop:
chr21:28325000-28350000~~chr21:42850000-42875000,
chr21:42300000-42325000~~chr21:42850000-42875000,
chr21:42575000-42600000~~chr21:42850000-42875000,
chr21:42592083-42595449~~chr21:42863770-42864944,
chr21:42850000-42875000~~chr21:43100000-43125000,
chr21:42850000-42875000~~chr21:43175000-43200000,
chr21:42850000-42875000~~chr21:43200000-43225000,
chr21:42850000-42875000~~chr21:43275000-43300000,
chr21:42850000-42875000~~chr21:43300000-43325000,
chr21:42850000-42875000~~chr21:43350000-43375000,
chr21:42850000-42875000~~chr21:43650000-43675000,
chr21:42850000-42875000~~chr21:43675000-43700000,
chr21:42875000-42900000~~chr21:43175000-43200000,
chr21:42875000-42900000~~chr21:43325000-43350000,
chr21:42875000-42900000~~chr21:43350000-43375000,
chr21:42875000-42900000~~chr21:43625000-43650000,
chr21:42875000-42900000~~chr21:43650000-43675000,
chr21:42875000-42900000~~chr21:43775000-43800000,
chr21:42875000-42900000~~chr21:44250000-44275000,
chr21:42875000-42900000~~chr21:44800000-44825000,
chr21:6475000-6500000~~chr21:42875000-42900000,