Variant report
Variant | rs4647388 |
---|---|
Chromosome Location | chr9:98049639-98049640 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:98046200-98050200 | Enhancers | Liver | Liver |
2 | chr9:98046600-98059400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
3 | chr9:98046600-98063000 | Weak transcription | Fetal Stomach | stomach |
4 | chr9:98047200-98059400 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
5 | chr9:98047400-98055800 | Weak transcription | HepG2 | liver |
6 | chr9:98048000-98055000 | Weak transcription | Fetal Intestine Small | intestine |
7 | chr9:98048200-98050200 | Enhancers | A549 | lung |
8 | chr9:98048600-98049800 | Enhancers | HSMMtube | muscle |
9 | chr9:98048800-98049800 | Weak transcription | NHLF | lung |
10 | chr9:98048800-98054400 | Weak transcription | Fetal Intestine Large | intestine |
11 | chr9:98048800-98059200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
12 | chr9:98049200-98051000 | Weak transcription | Small Intestine | intestine |
13 | chr9:98049200-98054400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
14 | chr9:98049600-98050000 | Enhancers | HSMM | muscle |