- Basic information
- CohesinDB ID: CDBP00420006
- Locus: chr21-41431562-41433383
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Data sourse: GSE93080, ENCSR000EAC, ENCSR000DZP, GSE67783, GSE86191, GSE105028, ENCSR000BMY, GSE103477, GSE50893
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Cell type: MDM, GM18526, HCT-116, SNYDER, GM19240, GM12878, GM2588, GM2255, HSPC, GM18486, H9-hESC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 3% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.878
- Subunit: SMC3,Rad21,SA1,SMC1
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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:
81% 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": 29%,
"5_TxWk": 27%,
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, PGR, SOX2, XBP1, FOXA1, HDGF, NFIC, RUNX3, CHD7, CBFB, PAX5, HDAC3, ELF1, BCLAF1, TEAD1, TRIM28, ZNF217, ESR1, SMAD5, CTCF, TCF12, BAF155, DPF2, PAX8, IRF4, PRKDC, RBPJ, TFAP2C, EED, POU2F2, NANOG, ZSCAN5D, ZNF263, MYCN, POU5F1, MTA2, ZNF317, DUX4, NBN, HNF4G, ERG, PBX1, MYC, SMARCA4, RAD21, GRHL3, NKX3-1, IKZF1, TERF2, VDR, NR3C1, KMT2A, CREB1, FEZF1, SPI1, HDAC2, GATA2, GATAD2B, NCOA2, RUNX1, BCL6, SMC1A, SIN3A, ZFX, MEF2A, CREBBP, GATA4, GR, ARNT, DAXX, BACH1, ATF2, ETV6, PBX3, MED1, CSNK2A1, TERF1, PML, PIAS1, NCOA1, SETDB1, MAFK, SP1, BCL11A, HNF4A, ARID1A, ASH2L, BCOR, TCF3, FOXP1, NCOR2, MLLT1, STAG1, ZNF283, MEF2B, FOXA2, EBF1, CREM, HDAC6, ZBED1, GTF2B, WT1, ZBTB33, CDK9, HOXB13, YY1, RELA, ZNF19, TARDBP, BRG1, ZFP36, HIF1A, GATA3, BATF, TAL1, MAX, NRIP1, ZNF143, PLAG1, TLE3, NCOA3, NR2F1, MED, T, BHLHE40, AR, TAF1, RB1, BRD4, MAZ, ZNF440
- Target gene symbol (double-evidenced CRMs): MX1,ABCG1,TMPRSS2,WDR4,PCP4,FAM3B,B3GALT5,UMODL1,RIPK4,C2CD2,BACE2
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 134
- Number of somatic mutations (non-coding): 28
- Related genes and loops
- Related gene:
ENSG00000183778,
ENSG00000183036,
ENSG00000182240,
ENSG00000183844,
ENSG00000157601,
ENSG00000184012,
ENSG00000183421,
ENSG00000157617,
ENSG00000177398,
ENSG00000160179,
ENSG00000160193,
- Related loop:
chr21:39600000-39625000~~chr21:41425000-41450000,
chr21:39700000-39725000~~chr21:41425000-41450000,
chr21:39900000-39925000~~chr21:41425000-41450000,
chr21:40775000-40800000~~chr21:41425000-41450000,
chr21:40800000-40825000~~chr21:41425000-41450000,
chr21:41000000-41025000~~chr21:41425000-41450000,
chr21:41125000-41150000~~chr21:41425000-41450000,
chr21:41150000-41175000~~chr21:41425000-41450000,
chr21:41175000-41200000~~chr21:41425000-41450000,
chr21:41275000-41300000~~chr21:41425000-41450000,
chr21:41300000-41325000~~chr21:41425000-41450000,
chr21:41361000-41363181~~chr21:41425246-41427778,
chr21:41425000-41450000~~chr21:41525000-41550000,
chr21:41425000-41450000~~chr21:41550000-41575000,
chr21:41425000-41450000~~chr21:41575000-41600000,
chr21:41425000-41450000~~chr21:41600000-41625000,
chr21:41425000-41450000~~chr21:41725000-41750000,
chr21:41425000-41450000~~chr21:41750000-41775000,
chr21:41425000-41450000~~chr21:41925000-41950000,
chr21:41425000-41450000~~chr21:42125000-42150000,
chr21:41425000-41450000~~chr21:42200000-42225000,
chr21:41425000-41450000~~chr21:42250000-42275000,
chr21:41425000-41450000~~chr21:42825000-42850000,
chr21:41425000-41450000~~chr21:45125000-45150000,