Variant report
Variant | rs6650636 |
---|---|
Chromosome Location | chr18:28796618-28796619 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr18:28787200-28805600 | Weak transcription | Pancreas | Pancrea |
2 | chr18:28787600-28797000 | Weak transcription | Right Atrium | heart |
3 | chr18:28791400-28796800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
4 | chr18:28791400-28796800 | Weak transcription | Left Ventricle | heart |
5 | chr18:28791400-28805600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
6 | chr18:28792400-28796800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
7 | chr18:28796400-28798000 | Enhancers | HepG2 | liver |
8 | chr18:28796600-28796800 | Enhancers | Fetal Kidney | kidney |
9 | chr18:28796600-28797000 | Enhancers | Stomach Mucosa | stomach |
10 | chr18:28796600-28798000 | Enhancers | HUES6 Cell Line | embryonic stem cell |
11 | chr18:28796600-28798000 | Enhancers | Placenta | Placenta |