Variant report
Variant | rs55667160 |
---|---|
Chromosome Location | chr7:96642685-96642686 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:96625000-96644000 | Bivalent/Poised TSS | Fetal Brain Female | brain |
2 | chr7:96628000-96643200 | Bivalent/Poised TSS | Brain Germinal Matrix | brain |
3 | chr7:96637200-96643400 | Bivalent/Poised TSS | Ganglion Eminence derived primary cultured neurospheres | brain |
4 | chr7:96639400-96644400 | Weak transcription | HepG2 | liver |
5 | chr7:96641400-96645000 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
6 | chr7:96642000-96642800 | Bivalent Enhancer | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
7 | chr7:96642000-96644200 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
8 | chr7:96642200-96643200 | Bivalent/Poised TSS | Cortex derived primary cultured neurospheres | brain |