Variant report
Variant | rs72913598 |
---|---|
Chromosome Location | chr1:59295289-59295290 |
allele | A/G |
Outlinks | Ensembl   UCSC |
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 |