Variant report
Variant | rs10485272 |
---|---|
Chromosome Location | chr6:102039357-102039358 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:102036600-102040800 | Weak transcription | Fetal Heart | heart |