Variant report
| Variant | rs1948982 |
|---|---|
| Chromosome Location | chr1:69593110-69593111 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:69586400-69596800 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
| 2 | chr1:69588800-69593600 | Weak transcription | Colon Smooth Muscle | Colon |
| 3 | chr1:69589000-69593400 | Weak transcription | Stomach Smooth Muscle | stomach |
| 4 | chr1:69592000-69594800 | Enhancers | Fetal Brain Male | brain |
| 5 | chr1:69592200-69593600 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
| 6 | chr1:69592400-69593200 | Enhancers | H1 Cell Line | embryonic stem cell |
| 7 | chr1:69592400-69593200 | Enhancers | Aorta | Aorta |
| 8 | chr1:69592400-69593200 | Enhancers | NHEK | skin |
| 9 | chr1:69592400-69593400 | Weak transcription | Fetal Brain Female | brain |
| 10 | chr1:69592400-69595600 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
| 11 | chr1:69593000-69593800 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
