Variant report
| Variant | rs1864963 |
|---|---|
| Chromosome Location | chr5:146892228-146892229 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr5:146890200-146895200 | Weak transcription | HUVEC | blood vessel |
| 2 | chr5:146890200-146901200 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
| 3 | chr5:146890200-146901200 | Weak transcription | NHLF | lung |
| 4 | chr5:146890200-146901600 | Weak transcription | NHDF-Ad | bronchial |
| 5 | chr5:146891400-146892400 | Enhancers | Fetal Muscle Trunk | muscle |
| 6 | chr5:146891800-146893200 | Enhancers | Colon Smooth Muscle | Colon |
| 7 | chr5:146892200-146892600 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 8 | chr5:146892200-146898800 | Weak transcription | Brain Germinal Matrix | brain |
