Variant report

Variant rs72913598
Chromosome Location chr1:59295289-59295290
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:59291000-59295800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr1:59291000-59296200 Weak transcription Ovary ovary
3 chr1:59291000-59298400 Weak transcription Placenta Amnion Placenta Amnion
4 chr1:59294000-59300400 Weak transcription Aorta Aorta
5 chr1:59294000-59301400 Weak transcription Left Ventricle heart
6 chr1:59294000-59311000 Weak transcription Gastric stomach
7 chr1:59294400-59295400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr1:59294400-59305600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:59295000-59296400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr1:59295000-59296400 Enhancers Osteobl bone
11 chr1:59295000-59296800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr1:59295000-59296800 Enhancers NHDF-Ad bronchial

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