Variant report

Variant rs73439635
Chromosome Location chr11:26248950-26248951
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:26241600-26249200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr11:26241600-26249800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr11:26248000-26250200 Enhancers HUVEC blood vessel
4 chr11:26248000-26251800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr11:26248400-26249000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr11:26248400-26249000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr11:26248400-26253400 Enhancers Hela-S3 cervix
8 chr11:26248400-26254000 Enhancers NHDF-Ad bronchial
9 chr11:26248600-26249000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr11:26248600-26249000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr11:26248600-26249200 Enhancers Fetal Brain Male brain
12 chr11:26248600-26251000 Enhancers HSMM muscle
13 chr11:26248600-26253400 Enhancers NHLF lung
14 chr11:26248600-26253800 Enhancers Muscle Satellite Cultured Cells --
15 chr11:26248600-26254000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr11:26248600-26254000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr11:26248600-26254000 Enhancers NHEK skin

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