Variant report
| Variant | rs34439296 |
|---|---|
| Chromosome Location | chr19:44223145-44223146 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr19:44216400-44223800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 2 | chr19:44216800-44223800 | Weak transcription | Hela-S3 | cervix |
| 3 | chr19:44218200-44232600 | Weak transcription | A549 | lung |
| 4 | chr19:44219600-44231600 | Weak transcription | Fetal Intestine Small | intestine |
| 5 | chr19:44220400-44223400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 6 | chr19:44220400-44240400 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 7 | chr19:44222200-44224400 | Enhancers | Placenta Amnion | Placenta Amnion |
| 8 | chr19:44222600-44223800 | Bivalent/Poised TSS | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 9 | chr19:44222800-44232800 | Weak transcription | H9 Cell Line | embryonic stem cell |
