- Basic information
- CohesinDB ID: CDBP00415903
- Locus: chr21-28227896-28231619
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Data sourse: ENCSR000EFJ, ENCSR230ZWH, GSE98367, GSE165895, ENCSR000HPG, ENCSR000BLY, GSE206145, GSE206145-NatGen2015, GSE120943, ENCSR000EDE, ENCSR000ECS, ENCSR917QNE
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Cell type: RPE, Fibroblast, Monocytes, HeLa-S3, IMR-90, SK-N-SH, Liver, Macrophage, HFFc6
- 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): 0.900
- Subunit: NIPBL,SA1,Rad21,SMC1,SA2,Mau2,SMC3
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CTCF binding site: CTCF
CTCF motif: False
- Genomic location: TSS
- 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:
35% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"15_Quies": 60%,
"7_Enh": 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: FOXO1, PGR, SMARCA2, E2F7, SOX2, NME2, FOXA1, HNRNPK, ATF3, NFIC, CHD7, CDX2, TEAD1, TRIM28, KLF6, ETV1, NFE2L2, ESR1, HNF1B, JUN, CTCF, TCF12, EP300, BAF155, GATA6, RFX5, TEAD4, PDX1, TFAP2C, POU5F1, CTBP1, DUX4, STAT1, ZNF300, ERG, HOXC5, MYC, SMARCA4, RFX1, RAD21, LHX2, TOP1, GRHL3, RXRA, BATF3, GABPA, STAT3, RCOR1, NFE2, VDR, ZNF750, CEBPB, NR3C1, ESRRA, KMT2A, CREB1, EBF3, ZHX2, SPI1, EHF, IRF1, GATA2, FLI1, MRTFB, NFYB, RUNX1, MAFG, SMC1A, CEBPA, LDB1, SMAD3, PCBP2, SMARCC1, MEF2A, RUNX2, GATA4, SP3, PBX4, ARNT, DAXX, BACH1, NRF1, ATF2, PBX3, MAFB, FOXM1, FOS, CDK8, MED1, CEBPD, PIAS1, SMAD1, C11orf30, TBX5, NUP98-HOXA9, MAFK, BCL11A, SP1, HNF4A, REST, ARID1A, ATF7, ZHX1, NCOR2, PPARG, FOXA2, CHD2, MAFF, MEF2C, ZBTB33, HOXB13, RELA, JUNB, BRG1, ISL1, GATA3, TAL1, MAX, GATA1, HAND2, TLE3, KLF4, TCF7L2, ZNF334, NFKB1, PHOX2B, AR, RNF2, BRD4, JUND, TBX2, ZNF316, FOSL2
- Target gene symbol (double-evidenced CRMs): ADAMTS1,LINC00113
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 20
- Related genes and loops
- Related gene:
ENSG00000154734,
ENSG00000225298,
- Related loop:
chr21:15575000-15600000~~chr21:28200000-28225000,
chr21:26800000-26825000~~chr21:28225000-28250000,
chr21:26825000-26850000~~chr21:28200000-28225000,
chr21:26825000-26850000~~chr21:28225000-28250000,
chr21:26875000-26900000~~chr21:28225000-28250000,
chr21:27300000-27325000~~chr21:28200000-28225000,
chr21:27300000-27325000~~chr21:28225000-28250000,
chr21:27550000-27575000~~chr21:28225000-28250000,
chr21:27750000-27775000~~chr21:28225000-28250000,
chr21:27825000-27850000~~chr21:28225000-28250000,
chr21:28050000-28075000~~chr21:28225000-28250000,
chr21:28075000-28100000~~chr21:28225000-28250000,
chr21:28100000-28125000~~chr21:28225000-28250000,
chr21:28125000-28150000~~chr21:28225000-28250000,
chr21:28200000-28225000~~chr21:28300000-28325000,
chr21:28200000-28225000~~chr21:28725000-28750000,
chr21:28225000-28250000~~chr21:28325000-28350000,
chr21:28225000-28250000~~chr21:28375000-28400000,
chr21:28225000-28250000~~chr21:28425000-28450000,
chr21:28225000-28250000~~chr21:28450000-28475000,
chr21:28225000-28250000~~chr21:28525000-28550000,
chr21:28225000-28250000~~chr21:28625000-28650000,
chr21:28225000-28250000~~chr21:28650000-28675000,
chr21:28225000-28250000~~chr21:28725000-28750000,
chr21:28225000-28250000~~chr21:28800000-28825000,