- Basic information
- CohesinDB ID: CDBP00419985
- Locus: chr21-41373113-41380866
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Data sourse: ENCSR000BLD, GSE206145-GSE177045, GSE104888, GSE72082, ENCSR000BSB, GSE116868, ENCSR000BLY, GSE105028, GSE121355, GSE103477, GSE131606, GSE108869, GSE25021, GSE115602, ENCSR000BTU, GSE93080, GSE67783, GSE86191, GSE138405, GSE76893, GSE206145-NatGen2015, GSE120943, GSE112028, ENCSR703TNG, GSE145327, GSE118494, GSE98367, ENCSR000BLS, GSE206145, ENCSR000ECE, GSE97394, ENCSR000BTQ, ENCSR167MTG, GSE110061, GSE129526, GSE111913, ENCSR054FKH, GSE68388, GSE126990, GSE50893, GSE126755, ENCSR000ECS, GSE38411
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Cell type: MDM, GM2610, HuCC-T1, H9-hESC, B-cell, GM2630, RPE, Fibroblast, Ishikawa, HeLa-S3, IMR-90, BCBL-1, GM18486, DKO, H1-hESC, Monocytes, MB157, GM12878, SK-N-SH, RT-112, HeLa-Tet-On, GM19099, HUES64, Macrophage, MCF-7, Hela-Kyoto, HCT-116, Hep-G2, GM19238, Neutrophil, HSPC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 19% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.656
- Subunit: SA1,Rad21,SMC1,SA2,Mau2,SMC3
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CTCF binding site: CTCF
CTCF motif: True
- Genomic location: Intragenic
- 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:
81% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"5_TxWk": 25%,
"4_Tx": 21%,
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: PGR, NME2, SUZ12, RBFOX2, ZFHX2, HDGF, ATF3, CTCFL, KLF14, TEAD1, SNAI2, ESR1, CTCF, JUN, KLF1, LMO1, SOX5, ZNF776, TFAP2C, BRD1, MYCN, ZNF263, TOP2A, ZBTB48, ZSCAN5A, DDX5, ERG2, OGG1, MYC, SMARCA4, RAD21, GRHL3, NKX2-1, GABPA, XRCC5, PRDM14, IKZF1, DNMT3B, NR3C1, ESRRA, EZH2, SPI1, RUNX1, SMC1A, SOX13, ZFX, TET2, ERG3, CREBBP, ZNF384, NOTCH1, RUNX2, GATA4, NRF1, ZNF48, PRDM9, FOS, ZEB1, MYB, ZMYM3, RBM22, BCL11A, FOXP1, AATF, ZNF623, SMC3, STAG1, TRP47, CBFA2T2, FOXA2, AGO1, EBF1, WT1, HOXB13, KDM1A, RELA, SP140, TCF4, TAL1, ZNF143, AGO2, CBX2, ZKSCAN8, NR2F1, ZNF334, ZSCAN22, EGR2, AR, HSF1, NCOR1, BRD4, MAZ, AHR
- Target gene symbol (double-evidenced CRMs): FAM3B,PRDM15,MX2,MX1,RIPK4,TMPRSS2,BACE2
- Function elements
- Human SNPs: Nevus_count_or_cutaneous_melanoma
- Number of somatic mutations (coding): 176
- Number of somatic mutations (non-coding): 144
- Related genes and loops
- Related gene:
ENSG00000182240,
ENSG00000183844,
ENSG00000183486,
ENSG00000157601,
ENSG00000184012,
ENSG00000183421,
ENSG00000141956,
- Related loop:
chr21:33400000-33425000~~chr21:41350000-41375000,
chr21:36525000-36550000~~chr21:41350000-41375000,
chr21:38775000-38800000~~chr21:41350000-41375000,
chr21:39175000-39200000~~chr21:41350000-41375000,
chr21:40925000-40950000~~chr21:41375000-41400000,
chr21:41125000-41150000~~chr21:41350000-41375000,
chr21:41150000-41175000~~chr21:41350000-41375000,
chr21:41169934-41171396~~chr21:41373764-41374984,
chr21:41275000-41300000~~chr21:41375000-41400000,
chr21:41350000-41375000~~chr21:41450000-41475000,
chr21:41350000-41375000~~chr21:41575000-41600000,
chr21:41350000-41375000~~chr21:41750000-41775000,
chr21:41350000-41375000~~chr21:41850000-41875000,
chr21:41350000-41375000~~chr21:43350000-43375000,
chr21:41367534-41370215~~chr21:41600536-41602815,
chr21:41368487-41370280~~chr21:41458627-41461687,
chr21:41368627-41370590~~chr21:41459655-41461711,
chr21:41368688-41370210~~chr21:41777426-41779194,
chr21:41368711-41370168~~chr21:41459737-41461655,
chr21:41368727-41370235~~chr21:41460007-41461704,
chr21:41375000-41400000~~chr21:41525000-41550000,
chr21:41375000-41400000~~chr21:43200000-43225000,