Variant report
Variant | rs10128686 |
---|---|
Chromosome Location | chr11:16148968-16148969 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:16145800-16149200 | Enhancers | HepG2 | liver |
2 | chr11:16146400-16149400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
3 | chr11:16147000-16149200 | Enhancers | Pancreatic Islets | Pancreatic Islet |
4 | chr11:16147600-16149400 | Enhancers | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
5 | chr11:16147600-16149400 | Enhancers | Fetal Lung | lung |
6 | chr11:16147600-16149800 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
7 | chr11:16148400-16155600 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
8 | chr11:16148400-16160200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |