- Basic information
- CohesinDB ID: CDBP00421352
- Locus: chr21-45799954-45801669
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Data sourse: GSE67783, GSE86191, GSE72082, ENCSR054FKH, GSE116344
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Cell type: RH4, HCT-116, HSPC, Hep-G2
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 2% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.956
- Subunit: SA1,Rad21
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CTCF binding site: CTCF
CTCF motif: False
- Genomic location: Intragenic
- 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:
83% 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": 57%,
"14_ReprPCWk": 19%,
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, TRIM25, XBP1, FOXA1, SUZ12, RXRB, TFAP4, ZBTB7B, ATF3, THRB, ZFP64, MXD4, MECOM, TP63, TRIM28, ESR1, OCA2, CTCF, JUN, EP300, KLF1, E4F1, LMO1, SOX5, E2F4, FOXA3, ZNF175, GATAD2A, MLX, TFAP2C, POU2F2, CHD8, BRD1, MYCN, ZNF263, TOP2A, ZBTB48, ZSCAN5A, SAP130, ERG2, HNF4G, ZNF300, ERG, ASCL1, OGG1, MYC, SMARCA4, RAD21, GRHL3, RXRA, GABPA, STAT3, XRCC5, ZNF614, PRDM14, DNMT3B, NR2F6, NR3C1, HNRNPL, CREB1, EZH2, GRHL2, EBF3, GABPB1, SPI1, MIXL1, KLF17, HDAC2, GATA2, ZNF644, DRAP1, HCFC1R1, NFIL3, RUNX1, SMC1A, EZH2phosphoT487, SIRT6, SOX13, ZFX, TET2, ERG3, SP5, PRDM10, RARA, CREBBP, NOTCH1, TAF15, GATA4, ARNT, ZNF48, SMAD4, CHD1, FOS, TEAD3, MYB, SCRT2, ZNF3, SETDB1, SP1, HNF4A, IKZF5, REST, HNRNPLL, TCF3, FOXP1, GLIS2, AATF, SMC3, STAG1, NFATC3, TRP47, CBFA2T2, FOXA2, MIER2, ZNF600, WT1, KDM1A, YY1, RELA, NEUROD1, SP140, ZIC2, HIF1A, GATA3, TAL1, MAX, ZNF449, NRIP1, PLAG1, CBX2, BCL11B, ZNF141, NCOA3, NR2F1, NEUROG2, KDM5B, ZNF334, MYOD1, EGR2, PHOX2B, ELF3, AR, RXR, ZBTB42, HEXIM1, ZBTB26, HSF1, BRD4, JUND, MAZ, AHR
- Target gene symbol (double-evidenced CRMs): COL18A1,ADARB1,PCBP3,POFUT2,ITGB2,ITGB2-AS1,FAM207A,SLC19A1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 14
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000160255,
ENSG00000227039,
ENSG00000160256,
ENSG00000197381,
ENSG00000186866,
ENSG00000182871,
ENSG00000173638,
ENSG00000183570,
- Related loop:
chr21:44925000-44950000~~chr21:45800000-45825000,
chr21:44950000-44975000~~chr21:45800000-45825000,
chr21:44975000-45000000~~chr21:45800000-45825000,
chr21:45125000-45150000~~chr21:45800000-45825000,
chr21:45150000-45175000~~chr21:45800000-45825000,
chr21:45200000-45225000~~chr21:45800000-45825000,
chr21:45275000-45300000~~chr21:45800000-45825000,
chr21:45300000-45325000~~chr21:45800000-45825000,
chr21:45325000-45350000~~chr21:45800000-45825000,
chr21:45350000-45375000~~chr21:45800000-45825000,
chr21:45425000-45450000~~chr21:45800000-45825000,
chr21:45450000-45475000~~chr21:45800000-45825000,
chr21:45525000-45550000~~chr21:45800000-45825000,
chr21:45550000-45575000~~chr21:45775000-45800000,
chr21:45550000-45575000~~chr21:45800000-45825000,
chr21:45575000-45600000~~chr21:45800000-45825000,
chr21:45675000-45700000~~chr21:45800000-45825000,