- Basic information
- CohesinDB ID: CDBP00418090
- Locus: chr21-35427520-35430013
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Data sourse: ENCSR000BLD, GSE67783, GSE86191, GSE98367, ENCSR000BLY, GSE105028, GSE206145-NatGen2015, GSE120943, ENCSR153HNT, GSE68388, GSE83726, GSE103477, GSE116344, GSE165895
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Cell type: MDM, H1-hESC, Macrophage, Fibroblast, HCT-116, Monocytes, RH4, H9-hESC, SK-N-SH, K-562, HSPC, HuCC-T1, 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): 0.856
- Subunit: SA1,Rad21,SMC1,SA2,Mau2
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CTCF binding site: non-CTCF
CTCF motif: False
- Genomic location: Intergenic
- 3D genome
- TAD boundary: Boundary
- Chromatin hubs: Hub
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Hi-C loops: True
Hi-ChIP loops: True
ChIA-PET loops: True
- Compartment:
81% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): Enhancer
- Super enhancer (SEdb): False
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Chromatin annotation:
"15_Quies": 34%,
"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: FOXO1, PGR, XBP1, HLF, PBX2, MLL4, BMI1, NFIC, RUNX3, ZNF383, SMARCE1, MITF, SFPQ, ZNF467, JMJD1C, MAF, TEAD1, RBM39, LMO2, ESR1, OCA2, CTCF, TCF12, EP300, LMO1, TEAD4, KMT2B, NANOG, BRD1, POU5F1, MYCN, RUNX1T1, KDM4C, CDK7, CTBP1, ZBTB48, ZSCAN5A, ERG2, ERG, ETS1, MYC, EOMES, KDM4A, RAD21, FOXP2, GRHL3, RXRA, NKX2-1, PROX1, GABPA, STAT3, IKZF1, ARNTL, NR3C1, CEBPB, STAT5B, KMT2A, EZH2, SPI1, ZNF786, IRF1, RUNX1, SMC1A, CEBPA, EZH2phosphoT487, SIN3A, ZFX, SMAD3, CBX8, ERG3, TWIST1, PRDM10, ZNF384, NOTCH1, RUNX2, CDK6, SMAD2, ARNT, PBX3, FOS, CDK8, MED1, MYB, L3MBTL2, TBX5, USF1, BCL11A, REST, CTBP2, TCF3, STAG1, SKI, PPARG, MEIS1, WT1, MEF2C, TCF7, ZKSCAN1, RELA, JUNB, GATA3, TAL1, MAX, ZNF143, CBX2, CEBPG, BCL11B, NR2F2, TP53, PKNOX1, ZNF334, MYOD1, T, TBX21, BHLHE40, AR, HSF1, RNF2, NOTCH3, BRD4, MAZ
- Target gene symbol (double-evidenced CRMs): SMIM11A
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000205670,
- Related loop:
chr21:34350000-34375000~~chr21:35400000-35425000,
chr21:34350000-34375000~~chr21:35425000-35450000,
chr21:34675000-34700000~~chr21:35400000-35425000,
chr21:34700000-34725000~~chr21:35400000-35425000,
chr21:34725000-34750000~~chr21:35400000-35425000,
chr21:34750000-34775000~~chr21:35400000-35425000,
chr21:34775000-34800000~~chr21:35400000-35425000,
chr21:34800634-34802701~~chr21:35431208-35432504,
chr21:34875000-34900000~~chr21:35400000-35425000,
chr21:34900000-34925000~~chr21:35400000-35425000,
chr21:35025000-35050000~~chr21:35400000-35425000,
chr21:35050000-35075000~~chr21:35400000-35425000,
chr21:35200000-35225000~~chr21:35400000-35425000,
chr21:35400000-35425000~~chr21:35500000-35525000,
chr21:35400000-35425000~~chr21:35525000-35550000,
chr21:35400000-35425000~~chr21:35575000-35600000,
chr21:35400000-35425000~~chr21:35600000-35625000,
chr21:35400000-35425000~~chr21:35625000-35650000,
chr21:35400000-35425000~~chr21:35825000-35850000,
chr21:35400000-35425000~~chr21:35925000-35950000,
chr21:35400000-35425000~~chr21:36025000-36050000,
chr21:35425000-35450000~~chr21:35600000-35625000,
chr21:35425000-35450000~~chr21:35825000-35850000,
chr21:35425000-35450000~~chr21:35950000-35975000,
chr21:35431113-35432519~~chr21:35507406-35509556,
chr21:35431152-35432481~~chr21:35939353-35941240,
chr21:35431177-35432375~~chr21:35838785-35841072,
chr21:35431208-35432504~~chr21:35838718-35841129,