- Basic information
- CohesinDB ID: CDBP00413534
- Locus: chr21-15603827-15604974
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Data sourse: ENCSR000BTU, ENCSR853VWZ, GSE72082, ENCSR193NSH, GSE138405, GSE116344, GSE25021, GSE206145, GSE101921, GSE85526, GSE206145-NatGen2015, ENCSR000EDE, GSE68388, ENCSR703TNG, GSE126990, GSE108869, ENCSR000ECS, ENCSR217ELF
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Cell type: MCF-7, RPE, HMEC, Fibroblast, Hela-Kyoto, RH4, HEKn, Ishikawa, A-549, HeLa-S3, HuCC-T1
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 7% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.878
- Subunit: NIPBL,SA1,Rad21,SMC1,SA2,Mau2,SMC3
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CTCF binding site: non-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:
56% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): False
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Chromatin annotation:
"15_Quies": 76%,
"7_Enh": 17%,
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, ZNF660, SOX2, FOXA1, ZFHX2, TFAP4, ATF3, NFIC, PRDM1, SMARCE1, KLF5, TEAD1, KLF6, ZNF217, ESR1, USF2, CTCF, TCF12, JUN, EP300, KLF1, DPF2, RFX5, DEK, E2F4, SMC1, TEAD4, GTF2F1, TFAP2C, NANOG, POU5F1, CTBP1, STAT1, SRF, GATAD1, TBP, ERG, HOXC5, MYC, SMARCA4, RAD21, LHX2, PROX1, NKX2-1, GABPA, STAT3, RCOR1, ZNF750, CEBPB, NR3C1, CREB1, GRHL2, EHF, HDAC2, GATA2, FLI1, MXI1, MRTFB, MYF5, CBX1, SMC1A, EZH2phosphoT487, SIN3A, AFF4, SMAD3, ERG3, SMARCC1, TWIST1, ZXDC, CREBBP, PBX4, NFIB, FOXM1, FOS, CHD1, MED1, KLF9, TBX5, MAFK, ZHX1, ASH2L, SMC3, ELL2, NCOR2, STAG1, FOXA2, CHD2, ZNF692, GTF2B, MAFF, HOXB13, KDM1A, YY1, RELA, JUNB, HIF1A, OTX2, GATA3, MAX, NRIP1, HAND2, KLF4, TP53, PKNOX1, EGR2, PHOX2B, ELF3, BRD2, AR, PAX3-FOXO1, YAP1, BRD4, JUND, CUX1, BRCA1, AHR
- Target gene symbol (double-evidenced CRMs): BTG3,USP25
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000155313,
ENSG00000154640,
- Related loop:
chr21:14250000-14275000~~chr21:15575000-15600000,
chr21:14275000-14300000~~chr21:15575000-15600000,
chr21:14300000-14325000~~chr21:15575000-15600000,
chr21:14375000-14400000~~chr21:15575000-15600000,
chr21:14400000-14425000~~chr21:15575000-15600000,
chr21:14425000-14450000~~chr21:15575000-15600000,
chr21:14450000-14475000~~chr21:15575000-15600000,
chr21:14725000-14750000~~chr21:15575000-15600000,
chr21:14775000-14800000~~chr21:15575000-15600000,
chr21:14825000-14850000~~chr21:15575000-15600000,
chr21:14850000-14875000~~chr21:15575000-15600000,
chr21:14950000-14975000~~chr21:15575000-15600000,
chr21:15225000-15250000~~chr21:15575000-15600000,
chr21:15475000-15500000~~chr21:15575000-15600000,
chr21:15575000-15600000~~chr21:15800000-15825000,
chr21:15575000-15600000~~chr21:28200000-28225000,
chr21:15600000-15625000~~chr21:15700000-15725000,
chr21:15600000-15625000~~chr21:15800000-15825000,
chr21:15600000-15625000~~chr21:15825000-15850000,
chr21:15600000-15625000~~chr21:17600000-17625000,