- Basic information
- CohesinDB ID: CDBP00419306
- Locus: chr21-38846463-38848614
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Data sourse: ENCSR000BTU, GSE206145-GSE177045, ENCSR230ZWH, GSE67783, GSE138405, GSE111913, ENCSR000BLY, ENCSR879KXD, GSE206145, GSE206145-NatGen2015, ENCSR000EDE, ENCSR153HNT, GSE112028, GSE68388, GSE126990, GSE108869, GSE126755, ENCSR000ECS, ENCSR917QNE
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Cell type: MCF-7, RPE, Hela-Kyoto, Fibroblast, Ishikawa, HeLa-S3, RT-112, Liver, SK-N-SH, K-562, HeLa-Tet-On, Neutrophil, HSPC, HuCC-T1
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 6% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.844
- Subunit: NIPBL,SA1,Rad21,SMC1,SA2,Mau2,SMC3
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CTCF binding site: non-CTCF
CTCF motif: False
- Genomic location: TSS,TES
- 3D genome
- TAD boundary: Boundary
- Chromatin hubs: non-Hub
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Hi-C loops: False
Hi-ChIP loops: False
ChIA-PET loops: True
- Compartment:
96% 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": 55%,
"7_Enh": 20%,
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: FOSL1, SOX2, MEIS2, XBP1, FOXA1, PBX2, UBTF, HDGF, ATF3, NFIC, TP63, MITF, KLF5, ETV1, ESR1, TP73, HDAC8, USF2, JUN, TCF12, CTCF, EP300, DPF2, E2F6, RFX5, CREB3, DEK, SOX6, RAD51, E2F4, DDX20, TEAD4, ZNF175, CHD8, MYCN, CTBP1, STAT1, TBP, HOXC5, ERG, ETS1, MYC, ONECUT1, SMARCA4, ARID1B, RAD21, FOXP2, RXRA, GABPA, STAT3, UBN1, RCOR1, DNMT3B, ZNF639, NFRKB, NR3C1, CEBPB, ZBTB11, EBF3, EHF, IRF1, HDAC2, GATA2, NCOA2, ATF1, CEBPA, HDAC1, ZFX, SMAD3, ERG3, ARNT, NRF1, BACH1, SOX11, PBX3, CBFA2T3, FOS, SMARCB1, TERF1, L3MBTL2, USF1, SP1, BCL11A, HNF4A, REST, PHIP, SMC3, NCOR2, STAG1, MLLT1, FOXA2, MTA3, CHD2, WT1, ZBTB33, ZNF589, YY1, RELA, JUNB, HIF1A, MGA, TAL1, MAX, GATA1, HAND2, PLAG1, KLF4, ZNF592, NCOA3, NR2F2, TCF7L2, NEUROG2, TP53, PKNOX1, NFKB1, BHLHE40, AR, HSF1, RNF2, NOTCH3, BRD4, JUND, MAZ, ZNF395
- Target gene symbol (double-evidenced CRMs): .
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
- Related loop:
chr21:27500000-27525000~~chr21:38850000-38875000,
chr21:38500000-38525000~~chr21:38850000-38875000,
chr21:38525000-38550000~~chr21:38850000-38875000,
chr21:38575000-38600000~~chr21:38850000-38875000,
chr21:38725000-38750000~~chr21:38850000-38875000,
chr21:38850000-38875000~~chr21:39050000-39075000,
chr21:38850000-38875000~~chr21:39100000-39125000,
chr21:38850000-38875000~~chr21:39150000-39175000,
chr21:38850000-38875000~~chr21:39400000-39425000,
chr21:38850000-38875000~~chr21:39600000-39625000,
chr21:38850000-38875000~~chr21:39850000-39875000,
chr21:38852714-38854659~~chr21:39125156-39127107,