Variant report
| Variant | rs1374888 |
|---|---|
| Chromosome Location | chr3:79050708-79050709 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr3:79040800-79062000 | Weak transcription | Ovary | ovary |
| 2 | chr3:79043200-79051800 | Weak transcription | Fetal Brain Male | brain |
| 3 | chr3:79044600-79051200 | Weak transcription | Brain Angular Gyrus | brain |
| 4 | chr3:79044600-79053800 | Weak transcription | Brain Germinal Matrix | brain |
| 5 | chr3:79044600-79061600 | Weak transcription | Fetal Kidney | kidney |
| 6 | chr3:79044800-79064600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 7 | chr3:79048000-79053000 | Weak transcription | HepG2 | liver |
| 8 | chr3:79048200-79054200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 9 | chr3:79048800-79052800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
