Variant report
Variant | rs16961569 |
---|---|
Chromosome Location | chr18:28842738-28842739 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr18:28837200-28845400 | Weak transcription | Liver | Liver |
2 | chr18:28840600-28842800 | Weak transcription | Stomach Mucosa | stomach |
3 | chr18:28841400-28844000 | Enhancers | Fetal Intestine Small | intestine |
4 | chr18:28841600-28844600 | Enhancers | Fetal Intestine Large | intestine |
5 | chr18:28841800-28843000 | Enhancers | Pancreas | Pancrea |
6 | chr18:28842000-28842800 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
7 | chr18:28842200-28842800 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
8 | chr18:28842200-28843800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
9 | chr18:28842200-28847400 | Weak transcription | GM12878-XiMat | blood |
10 | chr18:28842400-28849000 | Weak transcription | HepG2 | liver |
11 | chr18:28842600-28849200 | Weak transcription | Fetal Kidney | kidney |