Variant report
Variant | rs10205612 |
---|---|
Chromosome Location | chr2:212590258-212590259 |
allele | A/C |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:212569400-212590800 | Weak transcription | Fetal Kidney | kidney |
2 | chr2:212569600-212591800 | Weak transcription | Fetal Heart | heart |
3 | chr2:212571200-212594800 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
4 | chr2:212575600-212592000 | Weak transcription | Aorta | Aorta |
5 | chr2:212583600-212595400 | Weak transcription | Brain Anterior Caudate | brain |
6 | chr2:212586200-212590800 | Weak transcription | Brain Hippocampus Middle | brain |
7 | chr2:212587400-212595000 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
8 | chr2:212589800-212590400 | Enhancers | Brain Inferior Temporal Lobe | brain |
9 | chr2:212590200-212590400 | Flanking Active TSS | Brain Substantia Nigra | brain |