Variant report
Variant | rs73600560 |
---|---|
Chromosome Location | chr10:23183299-23183300 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:23181600-23185000 | Weak transcription | Gastric | stomach |
2 | chr10:23182200-23184400 | Enhancers | Fetal Intestine Small | intestine |
3 | chr10:23182200-23184600 | Enhancers | Foreskin Melanocyte Primary Cells skin01 | Skin |
4 | chr10:23182200-23184600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
5 | chr10:23182400-23183600 | Enhancers | Fetal Intestine Large | intestine |
6 | chr10:23182600-23184400 | Enhancers | Brain Hippocampus Middle | brain |
7 | chr10:23182800-23184600 | Enhancers | K562 | blood |
8 | chr10:23183000-23184000 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
9 | chr10:23183000-23184400 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
10 | chr10:23183200-23184000 | Enhancers | Primary Natural Killer cells fromperipheralblood | blood |