Variant report
Variant | rs55996712 |
---|---|
Chromosome Location | chr6:37768604-37768605 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:37766400-37768800 | Enhancers | Fetal Stomach | stomach |
2 | chr6:37766400-37775400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
3 | chr6:37767400-37768800 | Enhancers | HepG2 | liver |
4 | chr6:37767400-37775400 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
5 | chr6:37767400-37777000 | Weak transcription | Right Atrium | heart |
6 | chr6:37767800-37768800 | Weak transcription | Liver | Liver |
7 | chr6:37767800-37769600 | Weak transcription | Aorta | Aorta |
8 | chr6:37768400-37769000 | Enhancers | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
9 | chr6:37768600-37769000 | Enhancers | Cortex derived primary cultured neurospheres | brain |
10 | chr6:37768600-37769000 | Enhancers | Fetal Muscle Trunk | muscle |
11 | chr6:37768600-37769200 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
12 | chr6:37768600-37769200 | Enhancers | Fetal Kidney | kidney |