Variant report
Variant | rs56096758 |
---|---|
Chromosome Location | chr6:134433871-134433872 |
allele | A/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:134416200-134438600 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr6:134431400-134438000 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
3 | chr6:134431400-134438600 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
4 | chr6:134432800-134436800 | Enhancers | Brain Cingulate Gyrus | brain |
5 | chr6:134433800-134434000 | Enhancers | Primary neutrophils fromperipheralblood | blood |
6 | chr6:134433800-134434000 | Enhancers | Brain Dorsolateral Prefrontal Cortex | brain |
7 | chr6:134433800-134434400 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
8 | chr6:134433800-134434600 | Enhancers | Cortex derived primary cultured neurospheres | brain |
9 | chr6:134433800-134434600 | Enhancers | Brain Substantia Nigra | brain |
10 | chr6:134433800-134436400 | Enhancers | Brain Hippocampus Middle | brain |
11 | chr6:134433800-134437000 | Enhancers | Brain Inferior Temporal Lobe | brain |