Variant report
Variant | rs10887784 |
---|---|
Chromosome Location | chr10:89890801-89890802 |
allele | C/G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:89874000-89891400 | Weak transcription | Left Ventricle | heart |
2 | chr10:89878800-89892200 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
3 | chr10:89879200-89896600 | Weak transcription | H9 Cell Line | embryonic stem cell |
4 | chr10:89881200-89903800 | Weak transcription | Primary B cells from cord blood | blood |
5 | chr10:89886400-89891400 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
6 | chr10:89887600-89891400 | Weak transcription | Psoas Muscle | Psoas |
7 | chr10:89888800-89891800 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
8 | chr10:89889400-89891400 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
9 | chr10:89890800-89891200 | Enhancers | Skeletal Muscle Female | skeletal muscle |
10 | chr10:89890800-89892400 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
11 | chr10:89890800-89892400 | Enhancers | HMEC | breast |
12 | chr10:89890800-89892400 | Enhancers | NHEK | skin |