- Basic information
- CohesinDB ID: CDBP00414961
- Locus: chr21-23400845-23402059
-
Data sourse: ENCSR000BLD, GSE206145-GSE177045, GSE72082, GSE126634, ENCSR000BLY, GSE105028, GSE103477, GSE111537, GSE25021, GSE108869, ENCSR917QNE, ENCSR000BTU, GSE93080, ENCSR000DZP, ENCSR000EAC, ENCSR000BKV, GSE115250, GSE138405, GSE76893, GSE101921, GSE152721, GSE206145-NatGen2015, ENCSR198ZYJ, GSE112028, GSE130135, ENCSR703TNG, GSE116344, GSE138105, GSE145327, GSE94872, ENCSR000EEG, GSE76815, GSE115248, ENCSR000BLS, ENCSR000EHW, GSE206145, ENCSR000ECE, ENCSR000EHX, GSE97394, GSE55407, ENCSR000BTQ, GSE105004, GSE110061, GSE129526, GSE155324, ENCSR000EDE, GSE126990, GSE50893, ENCSR000ECS, GSE131577
-
Cell type: MDM, RH4, GM10847, GM2610, SLK, GM19240, Liver, TC-32, H9-hESC, RPE, GM2630, Fibroblast, Ishikawa, Kelly, GM12890, HeLa-S3, GM2255, K-562, GM18486, GM18526, H1-hESC, SNYDER, GM18505, Lymphoblast, GM12878, GM12891, GM2588, SK-N-SH, GM19239, HeLa-Tet-On, GM19193, HAP1, GM19099, HUES64, MCF-7, THP-1, Hela-Kyoto, HCT-116, HL-60, HEK293T, Hep-G2, MCF-10A, Neurons-H1, HUVEC, HCAEC, GM19238, HeLa, CNCC-WT33iPSC, OCI-AML-3, GM18951
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 26% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.444
- Subunit: SA1,Rad21,SMC1,SMC3ac,SA2,SMC3
-
CTCF binding site: CTCF
CTCF motif: True
- Genomic location: Intragenic
- 3D genome
- TAD boundary: Boundary
- Chromatin hubs: Hub
-
Hi-C loops: True
Hi-ChIP loops: True
ChIA-PET loops: True
- Compartment:
26% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): False
-
Chromatin annotation:
"15_Quies": 90%,
"9_Het": 9%,
Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
-
Co-bound Transcriptional factors: NANOG, SMC1A, SOX2, FOXA1, SRF, ZNF654, HOXB13, YY1, ZNF384, RAD21, TEAD1, KDM5B, STAG1, ESR1, CTCF, JUN, USF1, IRF4, POU2F3, BRD4, SMC1, MRTFB, SMC3, STAG2
- Target gene symbol (double-evidenced CRMs): NCAM2
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 16
- Related genes and loops
- Related gene:
ENSG00000154654,
- Related loop:
chr21:21000000-21025000~~chr21:23375000-23400000,
chr21:21000000-21025000~~chr21:23400000-23425000,
chr21:21225000-21250000~~chr21:23375000-23400000,
chr21:21850000-21875000~~chr21:23400000-23425000,
chr21:21925000-21950000~~chr21:23375000-23400000,
chr21:22025000-22050000~~chr21:23375000-23400000,
chr21:22175000-22200000~~chr21:23375000-23400000,
chr21:22625000-22650000~~chr21:23375000-23400000,
chr21:22725000-22750000~~chr21:23375000-23400000,
chr21:22775000-22800000~~chr21:23375000-23400000,
chr21:22775000-22800000~~chr21:23400000-23425000,
chr21:22800000-22825000~~chr21:23375000-23400000,
chr21:22875000-22900000~~chr21:23375000-23400000,
chr21:22925000-22950000~~chr21:23375000-23400000,
chr21:22975000-23000000~~chr21:23375000-23400000,
chr21:23100000-23125000~~chr21:23375000-23400000,
chr21:23100000-23125000~~chr21:23400000-23425000,
chr21:23125000-23150000~~chr21:23375000-23400000,
chr21:23125000-23150000~~chr21:23400000-23425000,
chr21:23130560-23132009~~chr21:23400684-23402228,
chr21:23130765-23131981~~chr21:23400851-23402181,
chr21:23150000-23175000~~chr21:23375000-23400000,
chr21:23250000-23275000~~chr21:23375000-23400000,
chr21:23250000-23275000~~chr21:23400000-23425000,
chr21:23275000-23300000~~chr21:23375000-23400000,
chr21:23375000-23400000~~chr21:23475000-23500000,
chr21:23375000-23400000~~chr21:24300000-24325000,
chr21:23375000-23400000~~chr21:25300000-25325000,
chr21:23400000-23425000~~chr21:23675000-23700000,
chr21:23400000-23425000~~chr21:23700000-23725000,
chr21:23400000-23425000~~chr21:23950000-23975000,
chr21:23400000-23425000~~chr21:24050000-24075000,
chr21:23400000-23425000~~chr21:24500000-24525000,
chr21:23400000-23425000~~chr21:25025000-25050000,
chr21:23400000-23425000~~chr21:26825000-26850000,