Variant report
Variant | rs28506968 |
---|---|
Chromosome Location | chr20:53171074-53171075 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr20:53162200-53172600 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
2 | chr20:53162400-53171600 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
3 | chr20:53166400-53177400 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
4 | chr20:53166800-53173600 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
5 | chr20:53166800-53176800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
6 | chr20:53167800-53174000 | Weak transcription | Osteobl | bone |
7 | chr20:53167800-53189200 | Weak transcription | Aorta | Aorta |
8 | chr20:53170800-53171600 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
9 | chr20:53170800-53172000 | Enhancers | H1 Cell Line | embryonic stem cell |
10 | chr20:53171000-53171200 | Enhancers | H9 Cell Line | embryonic stem cell |
11 | chr20:53171000-53171400 | Enhancers | Fetal Brain Female | brain |
12 | chr20:53171000-53171800 | Enhancers | iPS-18 Cell Line | embryonic stem cell |