Variant report
| Variant | rs6649018 |
|---|---|
| Chromosome Location | chrX:122598245-122598246 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chrX:122560000-122598800 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
| 2 | chrX:122583800-122614200 | Weak transcription | Brain Germinal Matrix | brain |
| 3 | chrX:122598000-122598400 | Enhancers | K562 | blood |
| 4 | chrX:122598000-122599400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 5 | chrX:122598000-122601400 | Weak transcription | Brain Inferior Temporal Lobe | brain |
| 6 | chrX:122598200-122599600 | Enhancers | HepG2 | liver |
