Variant report
Variant | rs1098497 |
---|---|
Chromosome Location | chr12:44709968-44709969 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:44699000-44712600 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
2 | chr12:44699000-44713800 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
3 | chr12:44699000-44736000 | Weak transcription | Pancreas | Pancrea |
4 | chr12:44699000-44782000 | Weak transcription | Aorta | Aorta |
5 | chr12:44703400-44711800 | Weak transcription | Fetal Intestine Small | intestine |
6 | chr12:44706800-44711800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
7 | chr12:44709200-44743200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |