Variant report
Variant | rs1198329 |
---|---|
Chromosome Location | chr13:50390096-50390097 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:50384200-50390200 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
2 | chr13:50386000-50390400 | Enhancers | HepG2 | liver |
3 | chr13:50387400-50394600 | Weak transcription | H9 Cell Line | embryonic stem cell |
4 | chr13:50387400-50394800 | Weak transcription | Fetal Intestine Large | intestine |
5 | chr13:50388800-50390200 | Enhancers | Foreskin Fibroblast Primary Cells skin02 | Skin |
6 | chr13:50389400-50390200 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
7 | chr13:50389400-50392800 | Weak transcription | Fetal Heart | heart |
8 | chr13:50390000-50394800 | Weak transcription | Placenta | Placenta |