- Basic information
- CohesinDB ID: CDBP00420097
- Locus: chr21-41667934-41670919
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Data sourse: ENCSR000BLD, GSE206145-GSE177045, GSE67783, GSE86191, GSE110061, GSE116868, GSE111913, GSE105028, GSE85526, GSE206145-NatGen2015, GSE206145, GSE131606
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Cell type: MCF-7, H1-hESC, RPE, Fibroblast, HCT-116, HEKn, MB157, DKO, RT-112, HSPC, H9-hESC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 4% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.878
- Subunit: SA1,Rad21,SMC1,SA2,Mau2
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CTCF binding site: CTCF
CTCF motif: False
- Genomic location: Intergenic
- 3D genome
- TAD boundary: non-Boundary
- Chromatin hubs: Hub
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Hi-C loops: True
Hi-ChIP loops: True
ChIA-PET loops: True
- Compartment:
89% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"15_Quies": 42%,
"14_ReprPCWk": 24%,
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: ZNF468, FOXO1, FOSL1, PGR, NME2, XBP1, FOXA1, SUZ12, HDGF, ATF3, THAP1, RUNX3, PRDM1, ZNF444, CBFB, TP63, ZSCAN4, ZNF736, CDC5L, JMJD1C, KLF5, TEAD1, ELF1, SNAI2, ESR1, USF2, CTCF, JUN, TCF12, LMO1, DPF2, ZNF410, ZNF512B, ZNF175, GTF2F1, TFAP2C, GLIS1, NANOG, CHD8, POU2F2, ZSCAN5D, MYCN, ZNF263, RUNX1T1, POU5F1, BRD1, ZSCAN21, ZNF317, ZBTB48, ZSCAN5A, SRF, DDX5, ERG2, ARID3A, ERG, ASCL1, OGG1, MYC, EZH1, SMARCA4, RAD21, GRHL3, STAT3, XRCC5, APC, NKX3-1, IKZF1, DNMT3B, VDR, NR3C1, CREB1, ARHGAP35, BMPR1A, GRHL2, GABPB1, ZHX2, SPI1, IRF1, ZNF257, HDAC2, GATA2, GATAD2B, FLI1, RUNX1, SMC1A, CBX1, SIRT6, ZFX, TET2, ERG3, RARA, ZNF384, TAF15, RUNX2, GATA4, GR, ARNT, NFIB, ZNF48, PRDM9, NCAPH2, FOS, SMARCB1, KDM6B, MYB, SCRT2, BCL11A, REST, ZNF605, HNRNPLL, CTBP2, TCF3, BCOR, AATF, SMC3, STAG1, MLLT1, TRP47, ZNF283, CBFA2T2, AGO1, FOXA2, TBL1X, ZNF600, WT1, CDK9, HOXB13, ZKSCAN1, YY1, RELA, TARDBP, SP140, ZIC2, HIF1A, GATA3, TAL1, MAX, GATA1, ZNF143, PLAG1, ZNF512, NR2F1, TCF7L2, KDM5B, TP53, ZNF334, AR, RXR, ZNF366, EGR1, HEXIM1, TFIIIC, HSF1, NCOR1, BRD4, SCRT1, MAZ, AHR
- Target gene symbol (double-evidenced CRMs): TFF1,RSPH1,UMODL1,B3GALT5,TMPRSS3,TFF2,PKNOX1,SLC37A1,C2CD2,RIPK4
- Function elements
- Human SNPs: Non-melanoma_skin_cancer
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 14
- Related genes and loops
- Related gene:
ENSG00000183778,
ENSG00000183421,
ENSG00000157617,
ENSG00000177398,
ENSG00000160181,
ENSG00000160182,
ENSG00000160183,
ENSG00000160188,
ENSG00000160190,
ENSG00000160199,
- Related loop:
chr21:39625000-39650000~~chr21:41650000-41675000,
chr21:40925000-40950000~~chr21:41650000-41675000,
chr21:41611455-41613750~~chr21:41673188-41674352,
chr21:41650000-41675000~~chr21:41750000-41775000,
chr21:41650000-41675000~~chr21:41900000-41925000,
chr21:41650000-41675000~~chr21:41950000-41975000,
chr21:41650000-41675000~~chr21:42100000-42125000,
chr21:41650000-41675000~~chr21:42350000-42375000,
chr21:41650000-41675000~~chr21:42475000-42500000,
chr21:41650000-41675000~~chr21:43000000-43025000,
chr21:41650000-41675000~~chr21:43300000-43325000,
chr21:41650000-41675000~~chr21:43350000-43375000,
chr21:41663192-41664922~~chr21:41777395-41780196,
chr21:41663218-41664946~~chr21:41777401-41780002,
chr21:41673182-41674339~~chr21:41916134-41918303,