Variant report
| Variant | rs7719166 |
|---|---|
| Chromosome Location | chr5:112785540-112785541 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr5:112762000-112786000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 2 | chr5:112764600-112786400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 3 | chr5:112764800-112786800 | Weak transcription | NHEK | skin |
| 4 | chr5:112770600-112786800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 5 | chr5:112780400-112787400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 6 | chr5:112782200-112789600 | Enhancers | Fetal Stomach | stomach |
| 7 | chr5:112783800-112786000 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
| 8 | chr5:112784000-112787800 | Weak transcription | Fetal Heart | heart |
| 9 | chr5:112785400-112785800 | Weak transcription | Fetal Lung | lung |
