Variant report
| Variant | rs74105168 |
|---|---|
| Chromosome Location | chr13:98049917-98049918 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr13:97995400-98050200 | Weak transcription | Small Intestine | intestine |
| 2 | chr13:98028000-98056400 | Weak transcription | Psoas Muscle | Psoas |
| 3 | chr13:98039600-98054400 | Weak transcription | Primary T cells from cord blood | blood |
| 4 | chr13:98041400-98050200 | Weak transcription | Fetal Stomach | stomach |
| 5 | chr13:98041800-98050800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 6 | chr13:98042000-98052800 | Weak transcription | Fetal Muscle Leg | muscle |
| 7 | chr13:98044600-98059400 | Weak transcription | Left Ventricle | heart |
| 8 | chr13:98045400-98059400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 9 | chr13:98048200-98050200 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
| 10 | chr13:98048400-98052200 | Weak transcription | NHLF | lung |
| 11 | chr13:98049000-98050200 | Enhancers | Fetal Lung | lung |
| 12 | chr13:98049400-98050000 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
| 13 | chr13:98049400-98050000 | Active TSS | Stomach Smooth Muscle | stomach |
