- Basic information
- CohesinDB ID: CDBP00413434
- Locus: chr21-15164670-15165346
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Data sourse: ENCSR167MTG, GSE72082, ENCSR501LQA, ENCSR676MJK, GSE76893, ENCSR000BLS, GSE206145, ENCSR335RKQ, ENCSR054FKH, ENCSR000EDE, GSE68388, ENCSR703TNG, GSE108869, ENCSR000ECS, ENCSR217ELF
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Cell type: MCF-7, Hep-G2, HEK293T, A-549, HeLa-S3, HuCC-T1
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 4% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.933
- Subunit: NIPBL,SA1,Rad21,SMC1,SMC3
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CTCF binding site: non-CTCF
CTCF motif: False
- Genomic location: Intergenic
- 3D genome
- TAD boundary: non-Boundary
- Chromatin hubs: Hub
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Hi-C loops: True
Hi-ChIP loops: False
ChIA-PET loops: True
- Compartment:
52% 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": 79%,
"7_Enh": 15%,
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: NFIA, FOSL1, PGR, HMG20A, FOXA1, RXRB, KDM3A, ATF3, THRB, ZFP64, MXD4, TP63, CDX2, TEAD1, TRIM28, KLF6, SNAI2, RCOR2, ZNF217, ESR1, OCA2, JUN, EP300, BAF155, SOX5, TRIM24, FOXA3, ZNF175, GATAD2A, GTF2F1, RBPJ, TFAP2C, MLX, BRD3, TOP2A, CTBP1, STAT1, PPARGC1A, SAP130, GATAD1, HNF4G, ERG, HOXC5, MYC, HOMEZ, RAD21, RXRA, NKX2-1, GABPA, STAT3, MIER3, TERF2, NR2F6, RCOR1, VDR, ESRRA, CEBPB, CREB1, TBL1XR1, GRHL2, ZNF652, GABPB1, SPI1, MIXL1, EHF, TFE3, HDAC2, GATA2, ZNF644, DRAP1, ZGPAT, NFIL3, NCOA2, ETV5, THAP11, BCL6, SMC1A, CEBPA, SOX13, SMAD3, SP5, SMARCC1, MYBL2, RARA, CREBBP, PBX4, DAXX, ZNF48, SMAD4, FOXM1, NR2C1, FOS, HMGXB4, CDK8, MED1, TEAD3, ZEB1, NR1H2, SP1, HNF4A, NKX2-5, IKZF5, REST, POU2F3, ASH2L, FOXP1, SMC3, SKI, PPARG, FOXA2, CREM, CHD2, MIER2, KDM1A, RELA, JUNB, TCF4, HIF1A, GATA3, MAX, NRIP1, GATA1, CEBPG, KLF4, NR2F2, NR2F1, TP53, ZNF334, NFKB1, MYOD1, ELF3, PHF5A, KAT8, NFKBIZ, AR, ARID4B, RXR, ZBTB26, BRD4, JUND, AHR, FOSL2
- Target gene symbol (double-evidenced CRMs): HSPA13,RBM11,SAMSN1,NRIP1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 3
- Related genes and loops
- Related gene:
ENSG00000185272,
ENSG00000155304,
ENSG00000155307,
ENSG00000180530,
- Related loop:
chr21:14100000-14125000~~chr21:15150000-15175000,
chr21:14225000-14250000~~chr21:15150000-15175000,
chr21:14275000-14300000~~chr21:15150000-15175000,
chr21:14375000-14400000~~chr21:15150000-15175000,
chr21:14450000-14475000~~chr21:15150000-15175000,
chr21:14500000-14525000~~chr21:15150000-15175000,
chr21:14600000-14625000~~chr21:15150000-15175000,
chr21:14775000-14800000~~chr21:15150000-15175000,
chr21:14850000-14875000~~chr21:15150000-15175000,
chr21:14875000-14900000~~chr21:15150000-15175000,
chr21:14880552-14881691~~chr21:15164198-15165741,
chr21:14950000-14975000~~chr21:15150000-15175000,
chr21:14975000-15000000~~chr21:15150000-15175000,
chr21:15150000-15175000~~chr21:15250000-15275000,
chr21:15150000-15175000~~chr21:15275000-15300000,
chr21:15150000-15175000~~chr21:15425000-15450000,
chr21:15150000-15175000~~chr21:15450000-15475000,
chr21:15150000-15175000~~chr21:15475000-15500000,
chr21:15158984-15160931~~chr21:15205692-15207786,