Variant report
| Variant | rs1819692 |
|---|---|
| Chromosome Location | chr6:24188667-24188668 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:24153800-24200800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 2 | chr6:24172800-24194800 | Weak transcription | Fetal Intestine Large | intestine |
| 3 | chr6:24177800-24198400 | Weak transcription | A549 | lung |
| 4 | chr6:24181400-24189600 | Strong transcription | HepG2 | liver |
| 5 | chr6:24184200-24195200 | Weak transcription | Pancreas | Pancrea |
| 6 | chr6:24184600-24195000 | Weak transcription | Fetal Intestine Small | intestine |
| 7 | chr6:24186600-24196000 | Weak transcription | Fetal Kidney | kidney |
| 8 | chr6:24187000-24189400 | Weak transcription | Fetal Brain Male | brain |
