Variant report
| Variant | rs551546300 |
|---|---|
| Chromosome Location | chr12:7591451-7591452 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:7582600-7592200 | Weak transcription | Adipose Nuclei | Adipose |
| 2 | chr12:7586600-7592400 | Weak transcription | HMEC | breast |
| 3 | chr12:7587400-7592200 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 4 | chr12:7589000-7592200 | Weak transcription | HUVEC | blood vessel |
| 5 | chr12:7590000-7593400 | Active TSS | ES-I3 Cell Line | embryonic stem cell |
| 6 | chr12:7590200-7593200 | Active TSS | K562 | blood |
| 7 | chr12:7591000-7593600 | Active TSS | A549 | lung |
| 8 | chr12:7591200-7591600 | Flanking Active TSS | Placenta | Placenta |
| 9 | chr12:7591200-7591800 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
| 10 | chr12:7591200-7593200 | Active TSS | ES-WA7 Cell Line | embryonic stem cell |
| 11 | chr12:7591200-7593400 | Active TSS | HUES6 Cell Line | embryonic stem cell |
| 12 | chr12:7591400-7591600 | Bivalent/Poised TSS | iPS-15b Cell Line | embryonic stem cell |
| 13 | chr12:7591400-7591600 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 14 | chr12:7591400-7592200 | Weak transcription | NHEK | skin |
| 15 | chr12:7591400-7592400 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
