- Basic information
- CohesinDB ID: CDBP00417811
- Locus: chr21-34687732-34691121
-
Data sourse: GSE72082, ENCSR000BSB, ENCSR501LQA, ENCSR760NPX, ENCSR000EGW, ENCSR000BLY, ENCSR150EFU, GSE121355, GSE131606, ENCSR330ELC, GSE108869, GSE25021, ENCSR000BUC, ENCSR000DYE, GSE165895, GSE143937, GSE67783, ENCSR000BKV, GSE115250, GSE138405, GSE86191, GSE76893, GSE101921, ENCSR806UKK, GSE51234, GSE120943, GSE206145-NatGen2015, GSE112028, ENCSR199XBQ, ENCSR703TNG, GSE116344, GSE145327, ENCSR895JMI, GSE76815, ENCSR193NSH, ENCSR768DOX, ENCSR879KXD, ENCSR000EHW, GSE85526, ENCSR981FDC, ENCSR247LSH, ENCSR807WAC, ENCSR000EHX, ENCSR620NWG, ENCSR748MVX, ENCSR767DFK, GSE206145, ENCSR495WGO, ENCSR984DZW, ENCSR217ELF, ENCSR000BTQ, GSE105004, ENCSR853VWZ, ENCSR956LGB, ENCSR944ZCT, GSE110061, GSE129526, ENCSR676MJK, GSE111913, ENCSR335RKQ, ENCSR537EFT, ENCSR000EDE, ENCSR153HNT, GSE68388, GSE126990, GSE50893, ENCSR000ECS, ENCSR481YWD
-
Cell type: RH4, GM10847, GM19240, GP5d, TC-32, HuCC-T1, RPE, GM2630, HMEC, Fibroblast, HEKn, GM12890, HeLa-S3, GM2255, K-562, DKO, HFFc6, GM18526, Monocytes, GM18505, GM2588, SK-N-SH, GM19239, HeLa-Tet-On, GM19193, RT-112, MCF-7, GM12892, Hela-Kyoto, HCT-116, A-549, GM19238, HeLa, CNCC-WT33iPSC, HSPC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 34% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.611
- Subunit: SA1,Rad21,SMC1,SMC3ac,SA2,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: 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:
"14_ReprPCWk": 31%,
"15_Quies": 22%,
Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
-
Co-bound Transcriptional factors: FOXO1, PGR, PPARG, TBL1X, FOXA2, ZFX, XBP1, WT1, FOXA1, BCL3, YY1, RELA, ATF3, RUNX2, GRHL3, PBX4, STAT3, PBX3, NKX3-1, ZNF143, MED1, NR3C1, CEBPB, PDX1, ESR1, CTCF, SPI1, AR, NCOR1, BRD4, SCRT1, TCF3, CLOCK, MAZ, ZNF528, STAG1
- Target gene symbol (double-evidenced CRMs): SETD4,CLIC6,RUNX1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 40
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000159212,
ENSG00000159216,
ENSG00000185917,
- Related loop:
chr21:34675000-34700000~~chr21:34775000-34800000,
chr21:34675000-34700000~~chr21:34800000-34825000,
chr21:34675000-34700000~~chr21:34850000-34875000,
chr21:34675000-34700000~~chr21:34875000-34900000,
chr21:34675000-34700000~~chr21:35400000-35425000,
chr21:34675000-34700000~~chr21:35450000-35475000,
chr21:34675000-34700000~~chr21:35500000-35525000,
chr21:34675000-34700000~~chr21:35575000-35600000,
chr21:34675000-34700000~~chr21:35600000-35625000,
chr21:34675000-34700000~~chr21:35825000-35850000,
chr21:34675000-34700000~~chr21:35850000-35875000,
chr21:34675000-34700000~~chr21:35925000-35950000,
chr21:34675000-34700000~~chr21:35950000-35975000,
chr21:34675000-34700000~~chr21:36025000-36050000,
chr21:34675000-34700000~~chr21:36100000-36125000,
chr21:34692249-34694404~~chr21:35507719-35509586,
chr21:34692384-34694384~~chr21:35615361-35617172,
chr21:34692406-34694411~~chr21:35648041-35649435,
chr21:34692433-34694405~~chr21:35507807-35509535,
chr21:34692471-34694305~~chr21:35399887-35401439,
chr21:34692474-34694411~~chr21:35507809-35509924,
chr21:34692480-34694427~~chr21:35399614-35401619,
chr21:34692573-34694447~~chr21:35399848-35401817,
chr21:34692731-34694389~~chr21:35399881-35401571,