Variant report
| Variant | rs10489389 |
|---|---|
| Chromosome Location | chr1:210510287-210510288 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:210503200-210516800 | Weak transcription | Lung | lung |
| 2 | chr1:210503600-210546800 | Weak transcription | Fetal Intestine Small | intestine |
| 3 | chr1:210504200-210512800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 4 | chr1:210504400-210514800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 5 | chr1:210504400-210516400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 6 | chr1:210506600-210514000 | Weak transcription | Fetal Heart | heart |
| 7 | chr1:210506600-210515600 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
| 8 | chr1:210506800-210512800 | Weak transcription | Primary B cells from peripheral blood | blood |
| 9 | chr1:210507600-210513000 | Weak transcription | Primary T helper 17 cells PMA-I stimulated | -- |
| 10 | chr1:210507800-210512200 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
