Variant report
| Variant | rs370398679 |
|---|---|
| Chromosome Location | chr7:103019907-103019908 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:102989800-103021200 | Weak transcription | Fetal Heart | heart |
| 2 | chr7:103009000-103021000 | Weak transcription | Gastric | stomach |
| 3 | chr7:103009000-103021000 | Weak transcription | Pancreas | Pancrea |
| 4 | chr7:103009000-103021200 | Weak transcription | Fetal Lung | lung |
| 5 | chr7:103009000-103029200 | Weak transcription | Spleen | Spleen |
| 6 | chr7:103009200-103020800 | Weak transcription | HepG2 | liver |
| 7 | chr7:103010800-103021000 | Weak transcription | Duodenum Mucosa | Duodenum |
| 8 | chr7:103019000-103020000 | Enhancers | K562 | blood |
| 9 | chr7:103019600-103020400 | Enhancers | Primary monocytes fromperipheralblood | blood |
