- Basic information
- CohesinDB ID: CDBP00420297
- Locus: chr21-42283471-42284076
-
Data sourse: GSE206145, GSE86191
-
Cell type: RPE, HCT-116
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 1% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.978
- Subunit: Rad21
-
CTCF binding site: non-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:
88% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
-
Chromatin annotation:
"4_Tx": 32%,
"5_TxWk": 28%,
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, KDM4B, FOXA1, SUZ12, ZFHX2, TFAP4, ATF3, ZC3H8, CTCFL, ZBTB44, CHD7, CBFB, TP63, ZNF320, TEAD1, ELF1, ETV1, LMO2, ESR1, OCA2, JUN, CTCF, BAF155, KLF1, DPF2, E2F4, SMC1, TEAD4, PDX1, TFAP2C, GLIS1, POU2F2, BRD1, ZSCAN5D, MYCN, ZNF263, POU5F1, ID3, ZBTB48, ZSCAN5A, SRF, ERG2, ERG, OGG1, ETS1, MYC, ONECUT1, SMARCA4, RAD21, GRHL3, KLF12, STAT3, APC, NKX3-1, PRDM14, DNMT3B, NR3C1, SRSF3, CREB1, EZH2, KLF8, BMPR1A, GRHL2, SPI1, HDAC2, GATA2, FLI1, MRTFB, RUNX1, SMC1A, BCL6, CBX1, NKX2-2, SIRT6, ZFX, SMAD3, TET2, ERG3, CBX8, SMARCC1, RARA, ZNF384, ZBTB2, CREBBP, TAF15, RUNX2, FANCD2, ARNT, PRDM9, NCAPH2, CHD1, FOS, SMARCB1, TEAD3, ZEB1, KDM6B, SCRT2, PIAS1, ZNF3, NCOA1, SREBF2, USF1, HNF4A, REST, ARID1A, FOXP1, AATF, SMC3, STAG1, STAG2, TRP47, CBFA2T2, FOXA2, AGO1, EBF1, MTA3, SS18, ZNF600, WT1, CDK9, HOXB13, ZKSCAN1, KDM1A, YY1, RELA, KAT2B, BRG1, SP140, ZIC2, HIF1A, KLF15, TAL1, MAF1, MAX, NRIP1, ZNF143, CBX2, PLAG1, NR2F2, TCF7L2, NR2F1, KDM5B, TP53, ZNF334, ZSCAN22, NFKB1, EGR2, ELF3, AR, RXR, EGLN2, HEXIM1, EGR1, TFIIIC, HSF1, BRD4, SCRT1, MAZ, AHR
- Target gene symbol (double-evidenced CRMs): PDE9A,TMPRSS2,UMODL1,PRDM15,UBASH3A,C2CD2,ABCG1,MX1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 48
- Number of somatic mutations (non-coding): 8
- Related genes and loops
- Related gene:
ENSG00000157601,
ENSG00000184012,
ENSG00000141956,
ENSG00000157617,
ENSG00000177398,
ENSG00000160179,
ENSG00000160185,
ENSG00000160191,
- Related loop:
chr21:41450000-41475000~~chr21:42275000-42300000,
chr21:41575000-41600000~~chr21:42275000-42300000,
chr21:41600000-41625000~~chr21:42275000-42300000,
chr21:41825000-41850000~~chr21:42275000-42300000,
chr21:41850000-41875000~~chr21:42275000-42300000,
chr21:41900000-41925000~~chr21:42275000-42300000,
chr21:41950000-41975000~~chr21:42275000-42300000,
chr21:42125000-42150000~~chr21:42275000-42300000,
chr21:42150000-42175000~~chr21:42275000-42300000,
chr21:42163609-42165687~~chr21:42276252-42278586,
chr21:42275000-42300000~~chr21:42425000-42450000,
chr21:42275000-42300000~~chr21:42675000-42700000,
chr21:42275000-42300000~~chr21:42750000-42775000,
chr21:42275000-42300000~~chr21:42775000-42800000,
chr21:42275000-42300000~~chr21:43175000-43200000,