Variant report
| Variant | rs9484717 |
|---|---|
| Chromosome Location | chr6:143593994-143593995 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:143570800-143609200 | Weak transcription | Fetal Intestine Large | intestine |
| 2 | chr6:143583400-143606000 | Weak transcription | Fetal Intestine Small | intestine |
| 3 | chr6:143583800-143615400 | Weak transcription | K562 | blood |
| 4 | chr6:143589000-143607400 | Weak transcription | Aorta | Aorta |
| 5 | chr6:143591400-143605200 | Weak transcription | Liver | Liver |
| 6 | chr6:143592200-143605600 | Weak transcription | Adipose Nuclei | Adipose |
| 7 | chr6:143592600-143594600 | Weak transcription | HSMM | muscle |
| 8 | chr6:143592800-143595000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 9 | chr6:143593200-143606800 | Weak transcription | NHEK | skin |
| 10 | chr6:143593400-143607000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
