Variant report
Variant | rs61770439 |
---|---|
Chromosome Location | chr1:85249858-85249859 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:85241000-85263600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr1:85246000-85250600 | Weak transcription | Colon Smooth Muscle | Colon |
3 | chr1:85246200-85250200 | Weak transcription | Stomach Smooth Muscle | stomach |
4 | chr1:85246400-85250800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
5 | chr1:85246400-85250800 | Weak transcription | NHEK | skin |
6 | chr1:85246600-85250400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
7 | chr1:85246600-85250600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
8 | chr1:85246600-85250600 | Weak transcription | HMEC | breast |
9 | chr1:85248000-85251200 | Weak transcription | Fetal Heart | heart |
10 | chr1:85248200-85250600 | Weak transcription | Brain Cingulate Gyrus | brain |
11 | chr1:85248400-85250800 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
12 | chr1:85248400-85250800 | Weak transcription | Brain Hippocampus Middle | brain |