Variant report
Variant | rs1046712 |
---|---|
Chromosome Location | chr1:169510475-169510476 |
allele | A/C |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:169485400-169510600 | Weak transcription | Primary mononuclear cells fromperipheralblood | Blood |
2 | chr1:169496000-169515200 | Strong transcription | Liver | Liver |
3 | chr1:169498400-169524000 | Weak transcription | Placenta | Placenta |
4 | chr1:169499000-169519000 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
5 | chr1:169500200-169526800 | Weak transcription | Left Ventricle | heart |
6 | chr1:169504000-169515000 | Strong transcription | HepG2 | liver |
7 | chr1:169505800-169511000 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
8 | chr1:169505800-169534800 | Weak transcription | Primary T helper cells PMA-I stimulated | -- |
9 | chr1:169506000-169510800 | Weak transcription | Primary monocytes fromperipheralblood | blood |
10 | chr1:169506200-169542800 | Weak transcription | Right Ventricle | heart |
11 | chr1:169507000-169530800 | Strong transcription | Monocytes-CD14+_RO01746 | blood |
12 | chr1:169508800-169510800 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
13 | chr1:169508800-169513200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
14 | chr1:169509600-169515600 | Strong transcription | Primary T regulatory cells fromperipheralblood | blood |
15 | chr1:169510200-169515800 | Strong transcription | Primary T helper 17 cells PMA-I stimulated | -- |