- Basic information
- CohesinDB ID: CDBP00420563
- Locus: chr21-42989441-42990324
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Data sourse: GSE67783, GSE86191, GSE206145-NatGen2015, ENCSR153HNT, GSE165895
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Cell type: Fibroblast, HCT-116, K-562, HSPC, HFFc6
- 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): 0.944
- Subunit: SA1,Rad21,SA2,SMC1
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CTCF binding site: non-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: False
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:
"5_TxWk": 64%,
"15_Quies": 18%,
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, FOSL1, MEIS2, XBP1, TBL1X, PATZ1, FOXA1, PBX2, LEO1, TFAP4, HDGF, ATF3, ZFP64, ZNF362, THAP1, RUNX3, ATF4, MORC2, CBFB, ZNF189, SMARCE1, PAX5, MITF, ZNF629, ELF1, TRIM28, TEAD1, ETV1, NFE2L2, LMO2, ESR1, OCA2, SAP30, HDAC8, USF2, CTCF, TCF12, JUN, EP300, E4F1, MNT, GATA6, DPF2, PAX8, SOX4, E2F6, TRIM24, SOX6, DEK, E2F4, E2F1, ZNF528, ZNF350, SMC1, TEAD4, GATAD2A, GTF2F1, RBPJ, EED, GLIS1, POU2F2, CHD8, BRD1, ZSCAN5D, MYCN, POU5F1, BRD3, ID3, CTBP1, MTA2, ZBTB17, ZBTB48, ZSCAN21, ZSCAN5A, NONO, SRF, DDX5, NBN, ARID3A, ERG, ETS1, MYC, SMARCA4, ARID1B, RAD21, FOXP2, GRHL3, NKX2-1, FOXK2, GABPA, STAT3, IKZF1, RCOR1, NFE2, NR2F6, MIER3, ARNTL, DACH1, NR3C1, ESRRA, CEBPB, ZNF93, LEF1, SRSF3, KMT2A, CREB1, EZH2, GABPB1, ZHX2, SPI1, EHF, IRF1, HDAC2, GATA2, TAF9B, FLI1, MXI1, SMARCA5, MRTFB, NCOA2, ATF1, ETV5, PTBP1, RUNX1, BCL6, MAFG, HDAC1, CEBPA, LDB1, AFF4, ZFX, SIN3A, SMAD3, ZNF770, TET2, ZNF18, PRDM10, SMARCC1, ZNF384, NOTCH1, RUNX2, GATA4, ARNT, NRF1, PBX4, ATF2, HMGB2, HMBOX1, CBFA2T3, FOXM1, PBX3, FOS, CDK8, SMARCB1, SUPT5H, CHD1, MED1, CSNK2A1, TEAD3, PML, ZXDB, CEBPD, TERF1, SMAD1, SUPT16H, ZNF3, C11orf30, NCOA1, L3MBTL2, TBX5, KLF16, ZNF22, RBM22, USF1, BCL11A, MAFK, FOXA2, REST, ZBTB7A, ZNF479, CCNT2, ATF7, ZHX1, PHIP, BCOR, FOXP1, TCF3, AFF1, GLIS2, AATF, SMC3, MLLT1, STAG1, ZNF394, NFATC3, TRP47, CBFA2T2, PPARG, ZNF316, MTA3, CREM, MEIS1, PAF1, CHD2, ZNF600, ZSCAN16, RBBP5, WT1, MAFF, ZNF574, ZBTB33, HOXB13, MPHOSPH8, KDM1A, YY1, RELA, ZNF318, JUNB, NEUROD1, SP140, TCF4, SKIL, HIF1A, GATA3, TAL1, MAX, NRIP1, GATA1, AGO2, ZNF143, ZNF333, PLAG1, CEBPG, GFI1B, NR2F2, NCOA3, NR2F1, NEUROG2, KDM5B, TP53, ZBTB6, PKNOX1, MED, ZNF334, MYOD1, BRD2, BHLHE40, AR, ZBTB40, YAP1, ZNF324, MYNN, NCOR1, RNF2, BRD4, ILF3, ZBTB26, CLOCK, JUND, MAZ, HSF1, ZNF24, AHR, FOSL2
- Target gene symbol (double-evidenced CRMs): PFKL,DNMT3L,PKNOX1,RRP1B,UBE2G2,TRPM2,HSF2BP,SUMO3,UMODL1,CFAP410
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 8
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000177398,
ENSG00000160199,
ENSG00000160207,
ENSG00000160208,
ENSG00000142182,
ENSG00000141959,
ENSG00000160226,
ENSG00000142185,
ENSG00000184787,
ENSG00000184900,
- Related loop:
chr21:34350000-34375000~~chr21:42975000-43000000,
chr21:39625000-39650000~~chr21:42975000-43000000,
chr21:42050000-42075000~~chr21:42975000-43000000,
chr21:42975000-43000000~~chr21:43325000-43350000,
chr21:42975000-43000000~~chr21:43350000-43375000,
chr21:42975000-43000000~~chr21:43575000-43600000,
chr21:42975000-43000000~~chr21:43650000-43675000,
chr21:42975000-43000000~~chr21:44250000-44275000,
chr21:42975000-43000000~~chr21:44325000-44350000,
chr21:42975000-43000000~~chr21:44800000-44825000,