Variant report
Variant | rs11989556 |
---|---|
Chromosome Location | chr8:64518613-64518614 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:64515600-64519800 | Enhancers | Fetal Brain Male | brain |
2 | chr8:64517800-64518800 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
3 | chr8:64518000-64519400 | Flanking Active TSS | Fetal Brain Female | brain |
4 | chr8:64518400-64518800 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
5 | chr8:64518400-64518800 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
6 | chr8:64518400-64519000 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
7 | chr8:64518400-64519000 | Flanking Active TSS | Brain Germinal Matrix | brain |
8 | chr8:64518400-64519800 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
9 | chr8:64518600-64519400 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
10 | chr8:64518600-64520600 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |