Variant report

Variant rs9332619
Chromosome Location chr1:169500348-169500349
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169484800-169501000 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
2 chr1:169485400-169510600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
3 chr1:169487400-169501000 Weak transcription Right Ventricle heart
4 chr1:169491600-169500800 Strong transcription Primary T regulatory cells fromperipheralblood blood
5 chr1:169494000-169502800 Strong transcription HepG2 liver
6 chr1:169496000-169515200 Strong transcription Liver Liver
7 chr1:169498400-169524000 Weak transcription Placenta Placenta
8 chr1:169498600-169506200 Strong transcription Monocytes-CD14+_RO01746 blood
9 chr1:169498600-169507600 Weak transcription Pancreatic Islets Pancreatic Islet
10 chr1:169498800-169501600 Strong transcription Primary monocytes fromperipheralblood blood
11 chr1:169499000-169500600 Enhancers HUES64 Cell Line embryonic stem cell
12 chr1:169499000-169501800 Strong transcription Primary neutrophils fromperipheralblood blood
13 chr1:169499000-169504200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr1:169499000-169508400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr1:169499000-169519000 Weak transcription Primary T helper cells fromperipheralblood blood
16 chr1:169499800-169501800 Strong transcription Primary T helper 17 cells PMA-I stimulated --
17 chr1:169500000-169504600 Weak transcription Primary T helper cells PMA-I stimulated --
18 chr1:169500200-169526800 Weak transcription Left Ventricle heart

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