Variant report
Variant | rs6939342 |
---|---|
Chromosome Location | chr6:145695363-145695364 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:145693200-145695400 | Enhancers | Stomach Mucosa | stomach |
2 | chr6:145694000-145696000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr6:145694400-145698600 | Weak transcription | Aorta | Aorta |
4 | chr6:145694400-145698800 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
5 | chr6:145695000-145696200 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
6 | chr6:145695000-145698600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
7 | chr6:145695200-145695600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |