Variant report
| Variant | rs7785183 |
|---|---|
| Chromosome Location | chr7:79918921-79918922 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:79913400-79922000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr7:79914800-79923400 | Weak transcription | Muscle Satellite Cultured Cells | -- |
| 3 | chr7:79915000-79923600 | Weak transcription | NHLF | lung |
| 4 | chr7:79917800-79923200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 5 | chr7:79917800-79923200 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 6 | chr7:79918600-79923400 | Weak transcription | Osteobl | bone |
