Variant report

Variant rs4769795
Chromosome Location chr13:30565298-30565299
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:30565000-30565800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
2 chr13:30565000-30566400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr13:30565000-30566400 Enhancers HSMMtube muscle
4 chr13:30565000-30566600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr13:30565000-30566800 Enhancers NH-A brain
6 chr13:30565000-30566800 Enhancers Osteobl bone
7 chr13:30565000-30569000 Enhancers NHDF-Ad bronchial
8 chr13:30565000-30569400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr13:30565200-30566000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr13:30565200-30566400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr13:30565200-30566400 Enhancers NHEK skin
12 chr13:30565200-30566600 Enhancers HMEC breast
13 chr13:30565200-30566800 Enhancers HSMM muscle
14 chr13:30565200-30566800 Enhancers NHLF lung
15 chr13:30565200-30568600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr13:30565200-30569400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung

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