- Basic information
- CohesinDB ID: CDBP00417421
- Locus: chr21-33655194-33657906
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Data sourse: GSE104888, ENCSR230ZWH, GSE72082, ENCSR000BSB, ENCSR501LQA, ENCSR760NPX, ENCSR000BLY, ENCSR150EFU, GSE103477, GSE111537, GSE131606, ENCSR330ELC, GSE108869, ENCSR000BUC, ENCSR917QNE, ENCSR000EFJ, ENCSR000BTU, GSE165895, GSE67783, GSE138405, GSE76893, GSE101921, ENCSR806UKK, GSE135093, GSE120943, GSE206145-NatGen2015, GSE130135, ENCSR199XBQ, ENCSR895JMI, GSE98367, ENCSR193NSH, ENCSR768DOX, ENCSR879KXD, GSE206145, GSE85526, ENCSR981FDC, ENCSR247LSH, ENCSR807WAC, ENCSR748MVX, ENCSR767DFK, ENCSR495WGO, ENCSR984DZW, ENCSR217ELF, GSE55407, ENCSR853VWZ, ENCSR956LGB, ENCSR944ZCT, GSE110061, GSE129526, ENCSR000HPG, ENCSR676MJK, ENCSR335RKQ, ENCSR537EFT, ENCSR000EDE, ENCSR153HNT, GSE68388, GSE126990, ENCSR000ECS
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Cell type: MDM, Liver, HuCC-T1, RPE, HMEC, Fibroblast, HEKn, Ishikawa, HeLa-S3, IMR-90, K-562, HFFc6, DKO, Monocytes, SK-N-SH, THP-1, Macrophage, MCF-7, Hela-Kyoto, HCT-116, HEK293T, A-549, HCAEC, OCI-AML-3, HSPC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 21% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.722
- Subunit: NIPBL,SA1,Rad21,SMC1,SA2,Mau2,SMC3
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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: True
ChIA-PET loops: True
- Compartment:
88% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"5_TxWk": 38%,
"7_Enh": 37%,
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: FOSL1, PGR, ZNF391, BDP1, ZNF426, MEIS2, PATZ1, FOXA1, PBX2, HNRNPK, ATF3, NFIC, ZNF362, CHD7, PRDM1, ZNF189, SMARCE1, ZSCAN4, MITF, CDX2, JMJD1C, ZNF629, KLF5, TEAD1, KLF6, SNAI2, KLF10, ESR1, HNF1B, USF2, JUN, TCF12, CTCF, EP300, GATA6, PYGO2, DPF2, SOX4, RFX5, DEK, E2F1, TEAD4, PDX1, TFAP2C, GLIS1, NANOG, POU5F1, MYCN, ID3, CTBP1, ZSCAN21, ZBTB17, ZBTB48, SRF, NBN, ERG2, ARID3A, TBP, ERG, ZBTB21, HOXC5, MYC, SMARCA4, ZNF2, ARID1B, HOMEZ, RAD21, GRHL3, TSHZ1, RXRA, NKX2-1, STAT3, IKZF1, RCOR1, ZNF639, VDR, ZNF750, ESRRA, CEBPB, NR3C1, CREB1, KLF8, GRHL2, ZHX2, SPI1, ZNF664, EHF, IRF1, KLF17, HDAC2, GATA2, FLI1, MRTFB, NFYB, ZNF554, ZIM3, ATF1, RUNX1, SMC1A, ZBTB24, HDAC1, NKX2-2, ZNF335, ZFX, SIN3A, AFF4, SMAD3, ERG3, CBX8, SMARCC1, PRDM10, MEF2A, CREBBP, ZNF384, ZNF35, RUNX2, GATA4, OSR2, ZNF184, SP3, PBX4, DAXX, ATF2, ZEB2, ZNF518A, HMBOX1, PBX3, FOXM1, SP2, FOS, CDK8, NFYA, MED1, TEAD3, ZEB1, ZXDB, ZNF558, SUPT16H, NR1H2, GTF3C2, TBX5, SETDB1, USF1, BCL11A, NIPBL, SP1, HNF4A, MAFK, REST, ARID1A, RBM25, ATF7, ZHX1, PHIP, GLIS2, FOXP1, AFF1, PRDM6, ZNF623, SMC3, ELL2, STAG2, ZNF394, CBX3, FOXA2, CHD2, PAF1, ZNF600, ZNF692, GTF2B, WT1, MAFF, ZSCAN16, KDM1A, RELA, JUNB, SP140, TCF4, ZNF830, OTX2, GATA3, TAL1, MAX, GATA1, MTA1, PLAG1, KLF4, ZFP69B, SP7, GFI1B, TCF7L2, TP53, PKNOX1, BRD2, ELF3, BHLHE40, AR, ZBTB40, YAP1, ZNF366, NCOR1, RNF2, BRD4, JUND, ZSCAN23, ZNF24, FOSL2
- Target gene symbol (double-evidenced CRMs): ATP5PO,AP000311.1,ITSN1,SMIM11A,RCAN1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 135
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000249209,
ENSG00000205726,
ENSG00000241837,
ENSG00000205670,
ENSG00000159200,
- Related loop:
chr21:33650000-33675000~~chr21:33750000-33775000,
chr21:33650000-33675000~~chr21:33875000-33900000,
chr21:33650000-33675000~~chr21:33900000-33925000,
chr21:33650000-33675000~~chr21:34350000-34375000,
chr21:33650000-33675000~~chr21:34525000-34550000,