- Basic information
- CohesinDB ID: CDBP00412862
- Locus: chr21-10399955-10406392
-
Data sourse: ENCSR000BLD, GSE206145-GSE177045, GSE72082, GSE116868, ENCSR000EGW, ENCSR000BLY, GSE105028, ENCSR000ECS, GSE121355, GSE103477, GSE111537, GSE131606, GSE108869, ENCSR000EDW, GSE25021, ENCSR000BUC, GSE115602, ENCSR000BTU, GSE93080, GSE143937, GSE67783, ENCSR000BKV, GSE86191, GSE138405, GSE76893, GSE206145-NatGen2015, GSE112028, GSE130135, ENCSR703TNG, GSE116344, GSE138105, GSE145327, GSE80989, GSE94872, ENCSR895JMI, GSE118494, ENCSR000EEG, ENCSR879KXD, ENCSR000BLS, GSE206145, ENCSR000ECE, ENCSR247LSH, ENCSR807WAC, ENCSR767DFK, ENCSR217ELF, ENCSR000BTQ, GSE105004, ENCSR167MTG, ENCSR853VWZ, ENCSR956LGB, GSE55407, GSE110061, GSE129526, GSE111913, ENCSR054FKH, ENCSR000EDE, ENCSR153HNT, GSE68388, GSE83726, GSE126990, GSE50893, ENCSR748MVX, GSE38411
-
Cell type: RH4, SLK, HuCC-T1, H9-hESC, RPE, Fibroblast, Ishikawa, VU1199-F, HeLa-S3, IMR-90, BCBL-1, K-562, DKO, H1-hESC, GM18951, MB157, GM12878, SK-N-SH, GM19239, HeLa-Tet-On, RT-112, THP-1, GM19099, MCF-7, GM12892, Hela-Kyoto, HCT-116, HEK293T, Hep-G2, A-549, HUVEC, HeLa, OCI-AML-3, HSPC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 31% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.611
- Subunit: SA1,Rad21,SMC1,SA2,ESCO2,Mau2,SMC3
-
CTCF binding site: CTCF
CTCF motif: False
- Genomic location: TSS,TES,Intergenic
- 3D genome
- TAD boundary: non-Boundary
- Chromatin hubs: Hub
-
Hi-C loops: True
Hi-ChIP loops: False
ChIA-PET loops: True
- Compartment:
26% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
-
Chromatin annotation:
"9_Het": 54%,
"8_ZNF/Rpts": 33%,
Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
-
Co-bound Transcriptional factors: RXR, STAT3
- Target gene symbol (double-evidenced CRMs): TPTE
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 439
- Related genes and loops
- Related gene:
ENSG00000274391,
- Related loop:
chr21:10250000-10275000~~chr21:10400000-10425000,
chr21:10375000-10400000~~chr21:10525000-10550000,
chr21:10375000-10400000~~chr21:10550000-10575000,
chr21:10400000-10425000~~chr21:10525000-10550000,
chr21:10400000-10425000~~chr21:10575000-10600000,
chr21:10400000-10425000~~chr21:10600000-10625000,
chr21:10400000-10425000~~chr21:10625000-10650000,
chr21:10400000-10425000~~chr21:10750000-10775000,
chr21:10400000-10425000~~chr21:10800000-10825000,
chr21:10400000-10425000~~chr21:13350000-13375000,
chr21:5225000-5250000~~chr21:10375000-10400000,
chr21:5225000-5250000~~chr21:10400000-10425000,
chr21:5250000-5275000~~chr21:10400000-10425000,
chr21:7250000-7275000~~chr21:10400000-10425000,
chr21:7950000-7975000~~chr21:10400000-10425000,
chr21:8025000-8050000~~chr21:10400000-10425000,
chr21:8650000-8675000~~chr21:10400000-10425000,
chr21:8975000-9000000~~chr21:10400000-10425000,
chr21:9000000-9025000~~chr21:10400000-10425000,
chr21:9225000-9250000~~chr21:10400000-10425000,
chr21:9750000-9775000~~chr21:10400000-10425000,