- Basic information
- CohesinDB ID: CDBP00417749
- Locus: chr21-34533706-34535019
-
Data sourse: GSE206145-GSE177045, GSE67783, GSE86191, GSE98367, GSE116868, GSE111913, GSE206145, GSE206145-NatGen2015, ENCSR000BMY, ENCSR153HNT, GSE68388, GSE111537, GSE165895
-
Cell type: MCF-7, Macrophage, RPE, Fibroblast, HCT-116, MB157, GM12878, RT-112, K-562, OCI-AML-3, HSPC, HuCC-T1, HFFc6
- 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): 0.856
- Subunit: SA1,Rad21,SMC1,SA2,Mau2
-
CTCF binding site: CTCF
CTCF motif: False
- Genomic location: Intragenic
- 3D genome
- TAD boundary: non-Boundary
- Chromatin hubs: Hub
-
Hi-C loops: True
Hi-ChIP loops: True
ChIA-PET loops: True
- Compartment:
93% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
-
Chromatin annotation:
"15_Quies": 37%,
"5_TxWk": 31%,
Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
-
Co-bound Transcriptional factors: FOXO1, FOSL1, PGR, SOX2, NME2, XBP1, FOXA1, HDGF, ZNF90, ATF3, RUNX3, CHD7, PRDM1, CBFB, ZNF189, MECOM, PAX5, TP63, MITF, JMJD1C, MAF, ELF1, TRIM28, BCLAF1, TEAD1, LMO2, ESR1, OCA2, TP73, MLL, USF2, JUN, CTCF, TCF12, EP300, SND1, KLF1, GATA6, DPF2, PAX8, IRF4, E2F1, TEAD4, KMT2B, RBPJ, EED, TFAP2C, GLIS1, POU2F2, CHD8, MYCN, SRC, TOP2A, ID3, RUNX1T1, POU5F1, MTA2, CDK7, ZBTB48, ZSCAN5A, KDM4C, DUX4, MLLT3, SAP130, NBN, ERG, ETS1, EZH1, MYC, SMARCA4, RAD21, GRHL3, RXRA, BATF3, STAT3, XRCC5, APC, PRDM14, IKZF1, NFE2, HNRNPH1, VDR, NR3C1, CEBPB, ESRRA, STAT5B, KMT2A, EZH2, GRHL2, ZHX2, SPI1, GATA2, ZNF644, GATAD2B, MXD3, FLI1, RELB, MRTFB, NCOA2, RUNX1, SMC1A, CEBPA, LDB1, CRY1, SIN3A, ZFX, SOX13, ZNF534, SMAD3, TET2, SMARCC1, ZBTB2, CREBBP, ZNF384, RUNX2, GATA4, ARNT, DAXX, PBX4, PRDM9, FOXM1, PBX3, CDK8, MED1, ZEB1, TEAD3, MYB, ZMYM3, SUPT16H, ZNF3, TBX5, STAT5A, RBM22, SP1, BCL11A, NR4A1, HNF4A, ATF7, POU2F3, ZNF263, TCF3, SMC3, MLLT1, STAG1, NFATC3, PAX7, MEF2B, PPARG, TBL1X, ZNF316, EBF1, SS18, ZNF600, WT1, ESR2, MEF2C, CDK9, HOXB13, KDM1A, YY1, RELA, TARDBP, JUNB, SP140, ZIC2, HIF1A, SKIL, OTX2, GATA3, BATF, MAX, NRIP1, GATA1, TLE3, KLF4, NCOA3, NR2F2, NR2F1, KDM5B, TP53, ZNF687, MED, ZNF334, BRD2, ELF3, TBX21, BHLHE40, AR, YAP1, RXR, RB1, HSF1, NOTCH3, BRD4, IKZF2, JUND, MAZ, AHR, FOSL2
- Target gene symbol (double-evidenced CRMs): AP000311.1,RCAN1,SMIM11A,ATP5PO,RUNX1,ITSN1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 12
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000249209,
ENSG00000205726,
ENSG00000241837,
ENSG00000205670,
ENSG00000159200,
ENSG00000159216,
- Related loop:
chr21:27500000-27525000~~chr21:34525000-34550000,
chr21:33650000-33675000~~chr21:34525000-34550000,
chr21:33675000-33700000~~chr21:34525000-34550000,
chr21:33700000-33725000~~chr21:34525000-34550000,
chr21:33900000-33925000~~chr21:34525000-34550000,
chr21:33950000-33975000~~chr21:34525000-34550000,
chr21:34150000-34175000~~chr21:34525000-34550000,
chr21:34200000-34225000~~chr21:34525000-34550000,
chr21:34325000-34350000~~chr21:34525000-34550000,
chr21:34350000-34375000~~chr21:34525000-34550000,
chr21:34525000-34550000~~chr21:34800000-34825000,
chr21:34525000-34550000~~chr21:35200000-35225000,
chr21:34525000-34550000~~chr21:38275000-38300000,
chr21:34525000-34550000~~chr21:38750000-38775000,
chr21:34534100-34535436~~chr21:34766515-34767688,
chr21:7800000-7825000~~chr21:34525000-34550000,