Variant report
Variant | rs992196 |
---|---|
Chromosome Location | chr2:180289038-180289039 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:180284000-180292600 | Weak transcription | HepG2 | liver |
2 | chr2:180288400-180293600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |