- Basic information
- CohesinDB ID: CDBP00413644
- Locus: chr21-16069741-16074239
-
Data sourse: GSE116868, ENCSR000BLY, ENCSR000ECS, GSE25021, ENCSR000BUC, ENCSR917QNE, GSE165895, ENCSR000BTU, GSE86191, GSE115250, GSE138405, GSE101921, GSE152721, GSE206145-NatGen2015, GSE112028, GSE94872, ENCSR193NSH, ENCSR000EHW, GSE206145, ENCSR000EHX, ENCSR984DZW, ENCSR217ELF, GSE131956, ENCSR000EDE, GSE126990, ENCSR748MVX
-
Cell type: Liver, TC-32, RPE, Fibroblast, Ishikawa, HeLa-S3, HFFc6, MB157, GBM39, SK-N-SH, HeLa-Tet-On, MCF-7, Hela-Kyoto, HCT-116, HEK293T, A-549, HUVEC, HCAEC, HAP1
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 10% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.789
- Subunit: SA1,Rad21,SMC1,SA2,Mau2,SMC3
-
CTCF binding site: CTCF
CTCF motif: False
- Genomic location: Intragenic
- 3D genome
- TAD boundary: Boundary
- Chromatin hubs: Hub
-
Hi-C loops: True
Hi-ChIP loops: False
ChIA-PET loops: True
- Compartment:
42% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): Enhancer
- Super enhancer (SEdb): True
-
Chromatin annotation:
"15_Quies": 46%,
"7_Enh": 17%,
Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
-
Co-bound Transcriptional factors: FOXO1, PGR, ZNF660, SOX2, NME2, XBP1, FOXA1, ZNF90, NFIC, ZBTB44, CHD7, CDX2, MAF, KLF5, TEAD1, ZNF573, ESR1, HNF1B, PITX3, JUN, CTCF, TCF12, BAF155, EP300, RFX5, E2F1, TEAD4, RBPJ, GLIS1, POU2F2, CHD8, POU5F1, MYCN, TOP2A, ZBTB17, DUX4, SRF, ERG, HOXC5, ASCL1, MYC, SMARCA4, RAD21, FOXP2, TOP1, GABPA, STAT3, RCOR1, NR3C1, CEBPB, CREB1, EBF3, ZNF257, GATA2, FLI1, MXI1, HEXIM1-CDK9, MRTFB, MYF5, CTNNB1, ZBTB24, CEBPA, SIN3A, ZNF534, POU4F2, ERG3, SMARCC1, TWIST1, CREBBP, RUNX2, CDK6, PBX4, ARNT, ATF2, PBX3, FOS, CHD1, MED1, PIAS1, KLF9, ZNF41, NUP98-HOXA9, USF1, REST, POU2F3, STAG1, PAX7, FOXA2, TBL1X, CHD2, SS18, ZSCAN16, ZNF692, FOXF1, HOXB13, KDM1A, YY1, RELA, JUNB, BRG1, ISL1, HIF1A, OTX2, GATA3, MAX, HAND2, NR2F2, TCF7L2, NEUROG2, TP53, PKNOX1, ZNF334, PHOX2B, BHLHE40, AR, PAX3-FOXO1, TAF1, EGLN2, NOTCH3, JUND, BRD4, MAZ, TBX2, BRCA1, FOSL2
- Target gene symbol (double-evidenced CRMs): HSPA13
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 52
- Related genes and loops
- Related gene:
ENSG00000155304,
- Related loop:
chr21:14375000-14400000~~chr21:16050000-16075000,
chr21:15875000-15900000~~chr21:16075000-16100000,
chr21:16050000-16075000~~chr21:16275000-16300000,
chr21:16050000-16075000~~chr21:16325000-16350000,
chr21:16050000-16075000~~chr21:16575000-16600000,
chr21:16050000-16075000~~chr21:16750000-16775000,
chr21:16050000-16075000~~chr21:16825000-16850000,
chr21:16050000-16075000~~chr21:17050000-17075000,
chr21:16075000-16100000~~chr21:16175000-16200000,
chr21:16075000-16100000~~chr21:16225000-16250000,
chr21:16075000-16100000~~chr21:16275000-16300000,
chr21:16075000-16100000~~chr21:16300000-16325000,
chr21:16075000-16100000~~chr21:16325000-16350000,
chr21:16075000-16100000~~chr21:16450000-16475000,
chr21:16075000-16100000~~chr21:16550000-16575000,
chr21:16075000-16100000~~chr21:16575000-16600000,
chr21:16075000-16100000~~chr21:16600000-16625000,
chr21:16075000-16100000~~chr21:16775000-16800000,
chr21:16075000-16100000~~chr21:17125000-17150000,
chr21:16075000-16100000~~chr21:17250000-17275000,