- Basic information
- CohesinDB ID: CDBP00420200
- Locus: chr21-41951919-41960803
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Data sourse: ENCSR000BLD, GSE206145-GSE177045, GSE104888, ENCSR230ZWH, GSE72082, ENCSR000BSB, ENCSR501LQA, GSE116868, ENCSR760NPX, ENCSR000EGW, ENCSR000BLY, GSE126634, GSE25021, ENCSR150EFU, GSE105028, GSE121355, GSE111537, GSE131606, ENCSR330ELC, ENCSR000EDW, GSE108869, ENCSR000BUC, ENCSR917QNE, ENCSR000EFJ, ENCSR000BTU, GSE115602, GSE143937, GSE165895, GSE67783, ENCSR000BKV, GSE86191, GSE138405, GSE93080, GSE76893, GSE101921, GSE206145-NatGen2015, GSE120943, GSE112028, GSE130135, ENCSR703TNG, GSE116344, GSE138105, GSE94872, ENCSR895JMI, GSE118494, ENCSR000EEG, ENCSR338DUC, GSE98367, ENCSR193NSH, ENCSR768DOX, ENCSR879KXD, ENCSR000BLS, ENCSR000EHW, GSE85526, ENCSR981FDC, ENCSR247LSH, GSE206145, ENCSR000EHX, ENCSR748MVX, ENCSR767DFK, ENCSR495WGO, GSE97394, ENCSR217ELF, ENCSR000BTQ, ENCSR167MTG, ENCSR853VWZ, ENCSR956LGB, GSE131956, GSE110061, GSE129526, ENCSR000HPG, GSE111913, GSE155324, ENCSR054FKH, ENCSR537EFT, ENCSR000EDE, ENCSR153HNT, GSE68388, GSE83726, GSE126990, GSE50893, ENCSR000ECS, GSE38411
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Cell type: RH4, GM10847, GM2610, SLK, GM19240, HSPC, Liver, HuCC-T1, B-cell, H9-hESC, GM2630, HMEC, Fibroblast, RPE, HEKn, Ishikawa, GM12890, HeLa-S3, GM2255, IMR-90, BCBL-1, K-562, GM18486, DKO, HFFc6, GM18526, H1-hESC, SNYDER, Monocytes, GM18505, MB157, Lymphoblast, GM12878, GM12891, GM2588, GBM39, SK-N-SH, GM19239, HeLa-Tet-On, GM19193, RT-112, HAP1, GM19099, HUES64, Macrophage, GM12892, MCF-7, Hela-Kyoto, HCT-116, MCF-10A, HEK293T, Hep-G2, A-549, HUVEC, HCAEC, GM19238, OCI-AML-3, GM18951
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 52% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.344
- Subunit: NIPBL,SA1,Rad21,SMC1,SA2,Mau2,SMC3
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CTCF binding site: CTCF
CTCF motif: False
- Genomic location: TSS,Intergenic
- 3D genome
- TAD boundary: non-Boundary
- Chromatin hubs: non-Hub
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Hi-C loops: True
Hi-ChIP loops: True
ChIA-PET loops: True
- Compartment:
96% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"7_Enh": 25%,
"2_TssAFlnk": 18%,
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, CHD8, AHR, MYCN, SP140, ZBTB26, ZBTB48, WT1, ZNF770, MAZ, FOS, TFAP2C
- Target gene symbol (double-evidenced CRMs): ZBTB21,UMODL1,C2CD2,PRDM15,ABCG1,BACE2,RSPH1,UBASH3A,SLC37A1
- Function elements
- Human SNPs: Total_testosterone_levels
- Number of somatic mutations (coding): 25
- Number of somatic mutations (non-coding): 54
- Related genes and loops
- Related gene:
ENSG00000182240,
ENSG00000141956,
ENSG00000157617,
ENSG00000173276,
ENSG00000177398,
ENSG00000160179,
ENSG00000160185,
ENSG00000160188,
ENSG00000160190,
- Related loop:
chr21:41200000-41225000~~chr21:41950000-41975000,
chr21:41425000-41450000~~chr21:41925000-41950000,
chr21:41600000-41625000~~chr21:41925000-41950000,
chr21:41600000-41625000~~chr21:41950000-41975000,
chr21:41611517-41613753~~chr21:41961729-41963240,
chr21:41650000-41675000~~chr21:41950000-41975000,
chr21:41775000-41800000~~chr21:41925000-41950000,
chr21:41850000-41875000~~chr21:41950000-41975000,
chr21:41925000-41950000~~chr21:42075000-42100000,
chr21:41925000-41950000~~chr21:42100000-42125000,
chr21:41925000-41950000~~chr21:42250000-42275000,
chr21:41925000-41950000~~chr21:43300000-43325000,
chr21:41925000-41950000~~chr21:43575000-43600000,
chr21:41950000-41975000~~chr21:42100000-42125000,
chr21:41950000-41975000~~chr21:42275000-42300000,
chr21:41950000-41975000~~chr21:42425000-42450000,
chr21:41950000-41975000~~chr21:42475000-42500000,
chr21:41952495-41953705~~chr21:42008731-42011959,
chr21:41957072-41959223~~chr21:42008838-42011899,
chr21:41957418-41959149~~chr21:42008452-42012075,