Variant report
| Variant | rs8005999 |
|---|---|
| Chromosome Location | chr14:77947925-77947926 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr14:77936200-77948600 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 2 | chr14:77940600-77948600 | Weak transcription | Fetal Kidney | kidney |
| 3 | chr14:77942400-77949000 | Weak transcription | Placenta | Placenta |
| 4 | chr14:77945000-77948800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 5 | chr14:77945000-77951800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 6 | chr14:77947200-77948000 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 7 | chr14:77947200-77956200 | Strong transcription | HepG2 | liver |
