Variant report
Variant | rs9767028 |
---|---|
Chromosome Location | chr6:145984548-145984549 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:145950800-145990600 | Weak transcription | Primary B cells from cord blood | blood |
2 | chr6:145951000-146003000 | Weak transcription | Thymus | Thymus |
3 | chr6:145951400-146003000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
4 | chr6:145973600-145990600 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
5 | chr6:145974200-146002800 | Weak transcription | Liver | Liver |
6 | chr6:145974800-146003600 | Weak transcription | Primary T helper naive cells fromperipheralblood | blood |
7 | chr6:145980600-146010800 | Weak transcription | Right Ventricle | heart |
8 | chr6:145982800-145989800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
9 | chr6:145982800-146003000 | Weak transcription | Primary B cells from peripheral blood | blood |
10 | chr6:145984400-145984600 | ZNF genes & repeats | Breast Myoepithelial Primary Cells | Breast |
11 | chr6:145984400-145989400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
12 | chr6:145984400-146003000 | Weak transcription | Primary hematopoietic stem cells | blood |