Variant report
Variant | rs182153532 |
---|---|
Chromosome Location | chr1:85295864-85295865 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:85288800-85296800 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
2 | chr1:85289400-85330800 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
3 | chr1:85291000-85296000 | Weak transcription | Right Ventricle | heart |
4 | chr1:85291000-85300000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
5 | chr1:85291200-85301000 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
6 | chr1:85291600-85296000 | Weak transcription | Left Ventricle | heart |
7 | chr1:85294400-85299400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
8 | chr1:85294600-85296200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
9 | chr1:85294600-85299200 | Weak transcription | HMEC | breast |
10 | chr1:85294600-85300400 | Weak transcription | Fetal Heart | heart |
11 | chr1:85295600-85296800 | Strong transcription | NHEK | skin |
12 | chr1:85295800-85296400 | Enhancers | Right Atrium | heart |
13 | chr1:85295800-85297000 | Strong transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |