Variant report
| Variant | rs3026924 |
|---|---|
| Chromosome Location | chr1:159110888-159110889 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:159110200-159111600 | Enhancers | H1 Cell Line | embryonic stem cell |
| 2 | chr1:159110200-159113400 | Active TSS | Fetal Brain Female | brain |
| 3 | chr1:159110400-159111800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 4 | chr1:159110600-159111400 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
| 5 | chr1:159110600-159112800 | Active TSS | Fetal Brain Male | brain |
| 6 | chr1:159110800-159111000 | Bivalent Enhancer | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 7 | chr1:159110800-159112200 | Active TSS | Brain Germinal Matrix | brain |
