- Basic information
- CohesinDB ID: CDBP00417240
- Locus: chr21-33206645-33209519
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Data sourse: GSE93080, ENCSR000EAC, ENCSR000DZP, ENCSR230ZWH, GSE104888, GSE86191, GSE138405, GSE98367, GSE76893, GSE62063, GSE120943, ENCSR153HNT, GSE50893, GSE126755, ENCSR917QNE
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Cell type: GM2610, Liver, GM2630, GM12890, GM2255, K-562, GM18486, GM18526, SNYDER, Monocytes, GM12878, GM12891, GM2588, GM19239, GM19193, GM19099, Macrophage, Ramos, GM12892, Hela-Kyoto, HCT-116, A-549, GM19238, Neutrophil, GM18951
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 9% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.722
- Subunit: NIPBL,SA1,Rad21,SMC1,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: True
ChIA-PET loops: True
- Compartment:
93% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"15_Quies": 45%,
"5_TxWk": 18%,
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: CBX5, XBP1, FOXA1, TFAP4, HDGF, THAP1, RUNX3, PAX5, ZNF287, JMJD1C, TRIM28, BCLAF1, ZNF26, ESR1, OCA2, CTCF, TCF12, ZNF695, DPF2, IRF4, TRIM24, SMC1, ZNF280A, EED, POU5F1, RUNX1T1, ZNF317, DUX4, ZSCAN5A, ZBTB48, STAT1, ZNF485, SMARCA4, RAD21, RXRA, STAT3, PRDM14, IKZF1, NFE2, HNRNPH1, VDR, NR3C1, CEBPB, KMT2A, SPI1, ZNF644, GATAD2B, RELB, NFIL3, RUNX1, SMC1A, BCL6, CEBPA, CBX1, ZFX, TRIM22, IRF2, CREBBP, ZNF184, ARNT, ZNF48, CDK8, MED1, TEAD3, TERF1, ZNF680, SETDB1, USF1, SP1, BCL11A, HNF4A, ATF7, TCF3, MLLT1, STAG1, MEF2B, CBX3, EBF1, ZNF662, MEF2C, CDK9, YY1, RELA, ZNF222, MAX, SPIB, ZNF143, KLF4, CEBPG, ZFP69B, NCOA3, NR2F1, ELF3, TBX21, EGR1, ZBTB26, NCOR1, IKZF2, JUND, BRD4, MAZ, ZNF316
- Target gene symbol (double-evidenced CRMs): IL10RB,RCAN1,IFNGR2,TMEM50B,SON,AP000311.1,SMIM11A,CRYZL1,ATP5PO,DONSON,ITSN1,IFNAR1,AP000295.1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 8
- Related genes and loops
- Related gene:
ENSG00000249624,
ENSG00000243646,
ENSG00000142166,
ENSG00000159128,
ENSG00000142188,
ENSG00000159140,
ENSG00000159147,
ENSG00000249209,
ENSG00000205758,
ENSG00000205726,
ENSG00000241837,
ENSG00000205670,
ENSG00000159200,
- Related loop:
chr21:29300000-29325000~~chr21:33200000-33225000,
chr21:33200000-33225000~~chr21:33300000-33325000,
chr21:33200000-33225000~~chr21:33325000-33350000,
chr21:33200000-33225000~~chr21:33350000-33375000,
chr21:33200000-33225000~~chr21:33375000-33400000,
chr21:33200000-33225000~~chr21:33400000-33425000,
chr21:33200000-33225000~~chr21:33425000-33450000,
chr21:33200000-33225000~~chr21:33450000-33475000,
chr21:33200000-33225000~~chr21:33550000-33575000,
chr21:33200000-33225000~~chr21:33575000-33600000,
chr21:33200000-33225000~~chr21:33600000-33625000,
chr21:33200000-33225000~~chr21:33800000-33825000,
chr21:33200000-33225000~~chr21:33875000-33900000,
chr21:33200000-33225000~~chr21:33900000-33925000,
chr21:33200000-33225000~~chr21:34350000-34375000,
chr21:33200000-33225000~~chr21:34600000-34625000,
chr21:33200000-33225000~~chr21:42225000-42250000,
chr21:33203382-33204703~~chr21:33228821-33231810,
chr21:33207409-33208640~~chr21:33308059-33310267,