Variant report
| Variant | rs10779552 |
|---|---|
| Chromosome Location | chr1:211429355-211429356 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:211421400-211430400 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 2 | chr1:211421600-211429800 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
| 3 | chr1:211421600-211429800 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
| 4 | chr1:211421800-211429800 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
| 5 | chr1:211421800-211430200 | Weak transcription | H1 Cell Line | embryonic stem cell |
| 6 | chr1:211421800-211430400 | Weak transcription | K562 | blood |
| 7 | chr1:211423200-211429800 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
| 8 | chr1:211423600-211430200 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 9 | chr1:211428600-211429800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
