- Basic information
- CohesinDB ID: CDBP00414412
- Locus: chr21-20442946-20444250
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Data sourse: ENCSR000BLD, GSE206145-GSE177045, ENCSR230ZWH, ENCSR000FAD, GSE72082, GSE126634, GSE116868, ENCSR000EGW, ENCSR000BLY, ENCSR404BPV, GSE105028, GSE121355, GSE103477, GSE111537, GSE131606, GSE108869, ENCSR000EDW, GSE25021, ENCSR917QNE, GSE115602, ENCSR000BTU, ENCSR000DZP, ENCSR000EAC, GSE143937, ENCSR000BKV, GSE115250, GSE138405, GSE67783, GSE86191, GSE76893, GSE101921, GSE152721, GSE51234, ENCSR198ZYJ, GSE112028, GSE130135, ENCSR703TNG, GSE106870, GSE116344, GSE138105, GSE145327, ENCSR000EEG, ENCSR879KXD, ENCSR000EHW, GSE206145, ENCSR000ECE, ENCSR000BMY, ENCSR000EHX, GSE97394, GSE55407, ENCSR000BTQ, GSE105004, ENCSR167MTG, GSE131956, GSE129526, GSE38411, ENCSR335RKQ, ENCSR000EDE, GSE68388, GSE83726, GSE126990, GSE50893, ENCSR000ECS, GSE131577
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Cell type: MDM, RH4, GM2610, SLK, CVB-hiPSC, HSPC, CVI-hiPSC, Liver, GP5d, TC-32, HuCC-T1, H9-hESC, RPE, GM2630, Ishikawa, HeLa-S3, GM2255, BCBL-1, K-562, GM18486, DKO, H1-hESC, SNYDER, MB157, GM12878, GM12891, GM2588, GBM39, SK-N-SH, GM19239, CNCCs-H9ESC, HeLa-Tet-On, THP-1, GM19099, HUES64, MCF-7, GM12892, Hela-Kyoto, HCT-116, HL-60, HEK293T, Hep-G2, MCF-10A, Neurons-H1, A-549, GM19238, HeLa, CNCC-WT33iPSC, OCI-AML-3, HAP1
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 33% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.433
- Subunit: SA1,Rad21,SMC1,SA2,SMC3
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CTCF binding site: CTCF
CTCF motif: True
- Genomic location: Intergenic
- 3D genome
- TAD boundary: Boundary
- Chromatin hubs: Hub
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Hi-C loops: True
Hi-ChIP loops: True
ChIA-PET loops: True
- Compartment:
23% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): False
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Chromatin annotation:
"15_Quies": 87%,
"9_Het": 13%,
Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
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Co-bound Transcriptional factors: RELA, AR, CDK2, POU2F2, CHD8, NCOA3, NEUROG2, ZFX, XBP1, ZBTB48, FOXA1, SETDB1, ZBTB33, STAG1
- Target gene symbol (double-evidenced CRMs): NCAM2
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 8
- Related genes and loops
- Related gene:
ENSG00000154654,
- Related loop:
chr21:18275000-18300000~~chr21:20425000-20450000,
chr21:18500000-18525000~~chr21:20425000-20450000,
chr21:18950000-18975000~~chr21:20425000-20450000,
chr21:19500000-19525000~~chr21:20425000-20450000,
chr21:19600000-19625000~~chr21:20425000-20450000,
chr21:19900000-19925000~~chr21:20425000-20450000,
chr21:20000000-20025000~~chr21:20425000-20450000,
chr21:20025000-20050000~~chr21:20425000-20450000,
chr21:20200000-20225000~~chr21:20425000-20450000,
chr21:20250000-20275000~~chr21:20425000-20450000,
chr21:20325000-20350000~~chr21:20425000-20450000,
chr21:20425000-20450000~~chr21:20525000-20550000,
chr21:20425000-20450000~~chr21:20550000-20575000,
chr21:20425000-20450000~~chr21:20650000-20675000,
chr21:20425000-20450000~~chr21:20875000-20900000,
chr21:20425000-20450000~~chr21:20950000-20975000,
chr21:20425000-20450000~~chr21:20975000-21000000,