Variant report
Variant | rs10481759 |
---|---|
Chromosome Location | chr9:86022917-86022918 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:86013400-86041000 | Weak transcription | Aorta | Aorta |
2 | chr9:86016600-86023600 | Weak transcription | HepG2 | liver |
3 | chr9:86017400-86034400 | Weak transcription | Psoas Muscle | Psoas |
4 | chr9:86019400-86037600 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
5 | chr9:86020800-86024200 | Enhancers | Primary neutrophils fromperipheralblood | blood |
6 | chr9:86021200-86041600 | Weak transcription | Right Ventricle | heart |
7 | chr9:86021800-86023000 | Flanking Active TSS | Monocytes-CD14+_RO01746 | blood |
8 | chr9:86022600-86023000 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
9 | chr9:86022600-86023000 | ZNF genes & repeats | Breast Myoepithelial Primary Cells | Breast |
10 | chr9:86022800-86023200 | ZNF genes & repeats | Fetal Muscle Leg | muscle |