Variant report
| Variant | rs1340695 |
|---|---|
| Chromosome Location | chr6:24316195-24316196 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:24314200-24321600 | Weak transcription | Fetal Heart | heart |
| 2 | chr6:24314400-24316200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 3 | chr6:24314400-24316200 | Weak transcription | HSMMtube | muscle |
| 4 | chr6:24314400-24321800 | Weak transcription | NH-A | brain |
| 5 | chr6:24315000-24319600 | Weak transcription | Fetal Kidney | kidney |
| 6 | chr6:24315600-24316400 | Enhancers | A549 | lung |
| 7 | chr6:24316000-24316400 | Enhancers | Pancreas | Pancrea |
| 8 | chr6:24316000-24316600 | ZNF genes & repeats | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 9 | chr6:24316000-24316600 | Genic enhancers | HepG2 | liver |
