Variant report
| Variant | rs540695873 |
|---|---|
| Chromosome Location | chr3:49587653-49587654 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr3:49585200-49590600 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 2 | chr3:49585400-49590600 | Weak transcription | H1 Cell Line | embryonic stem cell |
| 3 | chr3:49585800-49590400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 4 | chr3:49586000-49590800 | Weak transcription | Right Ventricle | heart |
| 5 | chr3:49587400-49588200 | Enhancers | HUVEC | blood vessel |
| 6 | chr3:49587400-49589800 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
| 7 | chr3:49587400-49590600 | Enhancers | HepG2 | liver |
| 8 | chr3:49587600-49587800 | Enhancers | Brain Inferior Temporal Lobe | brain |
| 9 | chr3:49587600-49587800 | Enhancers | Spleen | Spleen |
| 10 | chr3:49587600-49588400 | Enhancers | Cortex derived primary cultured neurospheres | brain |
| 11 | chr3:49587600-49590600 | Weak transcription | Right Atrium | heart |
