Variant report
Variant | rs1066394 |
---|---|
Chromosome Location | chr12:67719191-67719192 |
allele | A/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:67706600-67720600 | Weak transcription | Primary mononuclear cells fromperipheralblood | Blood |
2 | chr12:67711200-67721400 | Weak transcription | Fetal Brain Female | brain |
3 | chr12:67713400-67725000 | Weak transcription | Dnd41 | blood |
4 | chr12:67713600-67720800 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
5 | chr12:67716600-67732000 | Weak transcription | HMEC | breast |
6 | chr12:67716600-67748000 | Weak transcription | HSMM | muscle |
7 | chr12:67717000-67721400 | Weak transcription | Thymus | Thymus |
8 | chr12:67717400-67731400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
9 | chr12:67717600-67720800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
10 | chr12:67717800-67719400 | Weak transcription | HSMMtube | muscle |
11 | chr12:67718000-67720800 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
12 | chr12:67718200-67721000 | Weak transcription | Psoas Muscle | Psoas |