Variant report
| Variant | rs16843985 |
|---|---|
| Chromosome Location | chr3:101276747-101276748 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr3:101273000-101277600 | Weak transcription | H1 Cell Line | embryonic stem cell |
| 2 | chr3:101274600-101280400 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 3 | chr3:101276000-101280000 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
| 4 | chr3:101276400-101276800 | Active TSS | Fetal Adrenal Gland | Adrenal Gland |
| 5 | chr3:101276600-101276800 | Flanking Active TSS | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 6 | chr3:101276600-101276800 | Flanking Active TSS | K562 | blood |
| 7 | chr3:101276600-101277000 | Enhancers | HepG2 | liver |
| 8 | chr3:101276600-101280400 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
