Variant report
Variant | rs60119700 |
---|---|
Chromosome Location | chr2:167960781-167960782 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:167958600-167961000 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr2:167959800-167961000 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
3 | chr2:167960400-167961000 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
4 | chr2:167960600-167961400 | Enhancers | HepG2 | liver |
5 | chr2:167960600-167966200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |