- Basic information
- CohesinDB ID: CDBP00414108
- Locus: chr21-18244362-18246003
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Data sourse: ENCSR000BLD, GSE67783, GSE86191, GSE116868, ENCSR404BPV, GSE105028, GSE206145-NatGen2015, ENCSR000ECE, GSE206145, ENCSR198ZYJ, GSE38411
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Cell type: RPE, H1-hESC, Fibroblast, HCT-116, MB157, Neurons-H1, BCBL-1, HSPC, 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): 0.900
- Subunit: SA1,Rad21,SMC1,SA2,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: False
ChIA-PET loops: True
- Compartment:
31% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): False
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Chromatin annotation:
"13_ReprPC": 28%,
"10_TssBiv": 16%,
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, TRIM25, PGR, HMG20A, SOX2, XBP1, FOXA1, SUZ12, RING1B, ATF3, NFIC, CTCFL, CHD7, PRDM1, CBFB, MORC2, TP63, ZNF736, TEAD1, TRIM28, ELF1, ETV1, SNAI2, RBM39, RCOR2, ESR1, CTCF, TCF12, EP300, RYBP, E2F6, TRIM24, RAD51, SMC1, TEAD4, GATAD2A, EED, JARID2, NANOG, CHD8, BRD1, POU2F2, POU5F1, MYCN, TOP2A, KDM4C, BRD3, ZBTB17, ZBTB48, GATAD1, HNF4G, ERG, HOXC5, ASCL1, OGG1, MYC, SMARCA4, KDM4A, RAD21, GRHL3, PROX1, STAT3, XRCC5, PRDM14, NR2F6, NR3C1, KMT2A, CREB1, EZH2, GABPB1, PHF8, SPI1, HDAC2, ZNF644, MXD3, FLI1, MXI1, ETV5, RUNX1, SMC1A, EZH2phosphoT487, SIRT6, CRY1, ZNF335, ZFX, NFKBIA, SOX13, POU4F2, ZNF534, TET2, NMYC, TWIST1, RARA, ZNF701, BACH1, ZNF48, SMAD4, NCAPH2, MED1, ZEB1, TEAD3, KDM6B, L3MBTL2, SETDB1, BCL11A, HNF4A, ARID2, REST, ASH2L, HNRNPLL, CTBP2, BCOR, MBD2, FOXP1, AATF, SMC3, STAG1, TRP47, CBFA2T2, TBL1X, FOXA2, RBBP5, AGO1, MIER2, MAFF, CDK9, ZKSCAN1, KDM1A, YY1, RELA, NEUROD1, SP140, HIF1A, PCGF1, ZNF519, TAL1, MAX, MAF1, HAND2, TCF7L2, TP53, BRD2, AR, RXR, HEXIM1, TFIIIC, HSF1, RNF2, NOTCH3, BRD4, NCOR1, ZBTB26, AHR
- Target gene symbol (double-evidenced CRMs): TMPRSS15
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 141
- Number of somatic mutations (non-coding): 26
- Related genes and loops
- Related gene:
ENSG00000154646,
- Related loop:
chr21:17350000-17375000~~chr21:18250000-18275000,
chr21:17650000-17675000~~chr21:18225000-18250000,
chr21:17650000-17675000~~chr21:18250000-18275000,
chr21:17675000-17700000~~chr21:18225000-18250000,
chr21:17825000-17850000~~chr21:18225000-18250000,
chr21:17850000-17875000~~chr21:18225000-18250000,
chr21:17925000-17950000~~chr21:18250000-18275000,
chr21:18000000-18025000~~chr21:18225000-18250000,
chr21:18025000-18050000~~chr21:18225000-18250000,
chr21:18025000-18050000~~chr21:18250000-18275000,
chr21:18050000-18075000~~chr21:18225000-18250000,
chr21:18100000-18125000~~chr21:18250000-18275000,
chr21:18225000-18250000~~chr21:18325000-18350000,
chr21:18225000-18250000~~chr21:18500000-18525000,
chr21:18250000-18275000~~chr21:25300000-25325000,