Variant report
Variant | rs7702747 |
---|---|
Chromosome Location | chr5:114974415-114974416 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:114971600-114975400 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
2 | chr5:114971800-114976800 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
3 | chr5:114972000-114975600 | Enhancers | Cortex derived primary cultured neurospheres | brain |
4 | chr5:114972800-114976800 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
5 | chr5:114972800-114977000 | Weak transcription | H1 Cell Line | embryonic stem cell |
6 | chr5:114973600-114974600 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
7 | chr5:114973800-114974800 | Enhancers | GM12878-XiMat | blood |
8 | chr5:114974200-114977600 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
9 | chr5:114974400-114975200 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
10 | chr5:114974400-114976200 | Enhancers | Liver | Liver |
11 | chr5:114974400-114976400 | Enhancers | Pancreas | Pancrea |