Variant report
Variant | rs9805487 |
---|---|
Chromosome Location | chr13:39390861-39390862 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:39388800-39392600 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
2 | chr13:39389000-39397400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
3 | chr13:39389200-39393200 | Weak transcription | Pancreas | Pancrea |
4 | chr13:39389200-39404800 | Weak transcription | Gastric | stomach |
5 | chr13:39389400-39395800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
6 | chr13:39389400-39423000 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
7 | chr13:39390000-39392600 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
8 | chr13:39390000-39393000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
9 | chr13:39390000-39393000 | Weak transcription | HMEC | breast |
10 | chr13:39390000-39393000 | Weak transcription | NHEK | skin |
11 | chr13:39390000-39395800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
12 | chr13:39390200-39393200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |