Variant report
Variant | rs57065008 |
---|---|
Chromosome Location | chr12:44367563-44367564 |
allele | A/C |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:44343600-44376800 | Weak transcription | Pancreas | Pancrea |
2 | chr12:44356200-44368000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
3 | chr12:44358800-44367800 | Weak transcription | Esophagus | oesophagus |
4 | chr12:44361400-44401400 | Weak transcription | Aorta | Aorta |
5 | chr12:44363800-44382400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
6 | chr12:44364600-44369600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
7 | chr12:44364600-44370000 | Weak transcription | HMEC | breast |
8 | chr12:44364600-44393200 | Weak transcription | Small Intestine | intestine |
9 | chr12:44364800-44377000 | Weak transcription | Left Ventricle | heart |
10 | chr12:44366000-44375600 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
11 | chr12:44366200-44373400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
12 | chr12:44366600-44367800 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
13 | chr12:44366800-44368200 | Enhancers | Fetal Heart | heart |
14 | chr12:44367400-44368000 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |