Variant report
Variant | rs3745286 |
---|---|
Chromosome Location | chr19:41949870-41949871 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr19:41946000-41953000 | Weak transcription | Right Atrium | heart |
2 | chr19:41946600-41950800 | Weak transcription | Primary T helper naive cells fromperipheralblood | blood |
3 | chr19:41946800-41952400 | Weak transcription | Spleen | Spleen |
4 | chr19:41948000-41957200 | Weak transcription | Esophagus | oesophagus |
5 | chr19:41948800-41951000 | Active TSS | Fetal Intestine Large | intestine |
6 | chr19:41948800-41951000 | Active TSS | Fetal Intestine Small | intestine |
7 | chr19:41949200-41950600 | Active TSS | Duodenum Mucosa | Duodenum |
8 | chr19:41949200-41952400 | Weak transcription | Left Ventricle | heart |
9 | chr19:41949400-41953400 | Weak transcription | Primary monocytes fromperipheralblood | blood |
10 | chr19:41949600-41950400 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
11 | chr19:41949800-41950000 | Enhancers | Lung | lung |
12 | chr19:41949800-41950200 | Enhancers | GM12878-XiMat | blood |
13 | chr19:41949800-41955000 | Weak transcription | HepG2 | liver |