- Basic information
- CohesinDB ID: CDBP00414534
- Locus: chr21-21230579-21234343
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Data sourse: ENCSR000BLD, GSE206145-GSE177045, ENCSR230ZWH, ENCSR000FAD, GSE72082, GSE126634, GSE116868, GSE132649, ENCSR000BLY, ENCSR404BPV, GSE105028, GSE103477, GSE111537, GSE25021, GSE108869, ENCSR917QNE, ENCSR000EFJ, ENCSR000BTU, GSE115602, ENCSR000DZP, ENCSR000EAC, GSE139435, ENCSR000BKV, GSE115250, GSE138405, GSE143937, GSE76893, GSE101921, GSE135093, GSE152721, GSE206145-NatGen2015, ENCSR198ZYJ, GSE112028, GSE130135, ENCSR703TNG, GSE138105, GSE145327, GSE94872, ENCSR000EEG, GSE76815, GSE115248, ENCSR879KXD, ENCSR000BLS, ENCSR000EHW, GSE206145, ENCSR000ECE, GSE62063, ENCSR000BMY, ENCSR000EHX, ENCSR635OSG, ENCSR495WGO, GSE97394, GSE55407, ENCSR000BTQ, GSE105004, ENCSR167MTG, ENCSR956LGB, GSE129526, ENCSR000HPG, ENCSR000EDE, GSE68388, GSE126990, GSE50893, ENCSR000ECS, GSE131577
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Cell type: MDM, GM2610, SLK, Liver, TC-32, HuCC-T1, H9-hESC, RPE, GM2630, Fibroblast, Ishikawa, Kelly, HeLa-S3, IMR-90, K-562, GM18486, GM18526, H1-hESC, SNYDER, Leukemia-SEM, MB157, GM12878, GM12891, GM2588, SK-N-SH, GM19239, HeLa-Tet-On, THP-1, HUES64, MCF-7, Ramos, T-47D, Hela-Kyoto, HCT-116, HL-60, HEK293T, Hep-G2, MCF-10A, Neurons-H1, A-549, HUVEC, HCAEC, GM19238, HeLa, CNCC-WT33iPSC, OCI-AML-3, HAP1
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 39% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.467
- Subunit: NIPBL,SA1,Rad21,SMC1,SMC3ac,SA2,Mau2,SMC3
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CTCF binding site: CTCF
CTCF motif: True
- Genomic location: TSS,Intragenic
- 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:
27% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"15_Quies": 82%,
"7_Enh": 8%,
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: MIER1, REST, ONECUT1, IRF4, PIAS1, ARNT, HIF1A, DUX4, GABPA, STAT3, TEAD4, HOXB13, BAF155, EHMT2, ERG
- Target gene symbol (double-evidenced CRMs): NCAM2
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 55
- Number of somatic mutations (non-coding): 19
- Related genes and loops
- Related gene:
ENSG00000154654,
- Related loop:
chr21:21225000-21250000~~chr21:21350000-21375000,
chr21:21225000-21250000~~chr21:21450000-21475000,
chr21:21225000-21250000~~chr21:21475000-21500000,
chr21:21225000-21250000~~chr21:21500000-21525000,
chr21:21225000-21250000~~chr21:21600000-21625000,
chr21:21225000-21250000~~chr21:21675000-21700000,
chr21:21225000-21250000~~chr21:21900000-21925000,
chr21:21225000-21250000~~chr21:22100000-22125000,
chr21:21225000-21250000~~chr21:22525000-22550000,
chr21:21225000-21250000~~chr21:22775000-22800000,
chr21:21225000-21250000~~chr21:22875000-22900000,
chr21:21225000-21250000~~chr21:23375000-23400000,
chr21:21231430-21233404~~chr21:21920936-21923160,
chr21:21231477-21233381~~chr21:21687907-21690091,
chr21:21231521-21233402~~chr21:21687901-21690144,
chr21:21231528-21233140~~chr21:21688144-21689874,
chr21:21231535-21233401~~chr21:21687936-21689865,
chr21:21231535-21233401~~chr21:21920963-21923078,
chr21:21231535-21233410~~chr21:21920932-21923125,
chr21:21231541-21233362~~chr21:21920929-21923014,
chr21:21231560-21233379~~chr21:21687926-21689834,
chr21:21231560-21233379~~chr21:21920967-21923026,
chr21:21231567-21233381~~chr21:21921006-21922867,
chr21:21231594-21233378~~chr21:21688096-21689849,
chr21:21231694-21233389~~chr21:21687914-21690120,
chr21:21231694-21233389~~chr21:21920950-21923088,
chr21:21231825-21233156~~chr21:21921005-21922555,
chr21:21231867-21233358~~chr21:21688020-21689825,
chr21:21231867-21233358~~chr21:21921063-21923124,
chr21:21231916-21233147~~chr21:21688044-21689859,