- Basic information
- CohesinDB ID: CDBP00420021
- Locus: chr21-41479819-41481047
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Data sourse: GSE67783, ENCSR230ZWH, GSE86191, GSE116868, GSE105028, ENCSR917QNE
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Cell type: HCT-116, MB157, Liver, HSPC, H9-hESC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 2% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.944
- Subunit: SA1,Rad21,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: False
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): True
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Chromatin annotation:
"14_ReprPCWk": 24%,
"5_TxWk": 22%,
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: NFIA, PGR, SMARCA2, SOX2, XBP1, FOXA1, SUZ12, MLL4, ZFHX2, TFAP4, ATF3, NFIC, ZFP64, CHD7, RUNX3, MORC2, MECOM, MITF, KLF5, TEAD1, TRIM28, ELF1, SNAI2, SAP30, ESR1, LMO2, USF2, CTCF, TCF12, EP300, BAF155, SOX5, GATA6, RYBP, E2F6, IRF4, E2F1, ZNF528, TEAD4, ZNF175, PDX1, TFAP2C, RBPJ, NANOG, CHD8, BRD1, BRD3, POU5F1, TOP2A, CDK7, MYCN, ZNF263, ZBTB48, ZSCAN5A, STAT1, SRF, SAP130, ERG2, SP4, TBP, HNF4G, ERG, ZBTB21, ASCL1, MYC, SMARCA4, KDM4A, RAD21, RXRA, PROX1, GABPA, STAT3, XRCC5, PRDM14, NR3C1, CEBPB, ESRRA, HNRNPL, KMT2A, CREB1, EZH2, GRHL2, ZHX2, HDAC2, GATA2, MXD3, FLI1, HCFC1R1, MRTFB, NCOA2, ZNF554, RUNX1, BCL6, SMC1A, CEBPA, EZH2phosphoT487, SOX13, ZFX, SMAD3, TET2, ERG3, SMARCC1, CREBBP, RARA, NOTCH1, RUNX2, GATA4, ARNT, BACH1, PBX4, NFIB, ATF2, ZNF48, SMAD4, FOXM1, CHD1, HMGXB4, CDK8, FOS, MED1, TEAD3, ZEB1, KDM6B, MYB, USF1, SP1, NIPBL, BCL11A, HNF4A, TFAP2A, REST, ZBTB7A, ASH2L, CTBP2, TCF3, BCOR, FOXP1, SMC3, STAG1, TRP47, CBFA2T2, ZNF207, FOXA2, RBBP5, CHD2, HDAC6, SS18, ZNF600, WT1, ESR2, ZBTB33, CDK9, KDM1A, YY1, RELA, JUNB, SP140, ZIC2, HIF1A, PCGF1, TCF4, BHLHE22, GATA3, TAL1, MAX, NRIP1, ZNF143, CBX2, BCL11B, NCOA3, TCF7L2, NR2F1, KDM5B, TP53, ZNF334, MYOD1, EGR2, ELF3, T, AR, TAF1, YAP1, EGLN2, ZBTB26, HSF1, BRD4, JUND, MAZ, AHR
- Target gene symbol (double-evidenced CRMs): TMPRSS2
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 225
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000184012,
- Related loop:
chr21:40125000-40150000~~chr21:41450000-41475000,
chr21:41125000-41150000~~chr21:41450000-41475000,
chr21:41150000-41175000~~chr21:41450000-41475000,
chr21:41200000-41225000~~chr21:41450000-41475000,
chr21:41275000-41300000~~chr21:41450000-41475000,
chr21:41300000-41325000~~chr21:41450000-41475000,
chr21:41350000-41375000~~chr21:41450000-41475000,
chr21:41450000-41475000~~chr21:41575000-41600000,
chr21:41450000-41475000~~chr21:41600000-41625000,
chr21:41450000-41475000~~chr21:41700000-41725000,
chr21:41450000-41475000~~chr21:41750000-41775000,
chr21:41450000-41475000~~chr21:41825000-41850000,
chr21:41450000-41475000~~chr21:42100000-42125000,
chr21:41450000-41475000~~chr21:42125000-42150000,
chr21:41450000-41475000~~chr21:42275000-42300000,