Variant report
Variant | rs12077089 |
---|---|
Chromosome Location | chr1:85298014-85298015 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:85289400-85330800 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
2 | chr1:85291000-85300000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
3 | chr1:85291200-85301000 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
4 | chr1:85294400-85299400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
5 | chr1:85294600-85299200 | Weak transcription | HMEC | breast |
6 | chr1:85294600-85300400 | Weak transcription | Fetal Heart | heart |
7 | chr1:85296000-85300200 | Weak transcription | NHLF | lung |
8 | chr1:85296400-85299200 | Weak transcription | Pancreas | Pancrea |
9 | chr1:85296600-85299200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
10 | chr1:85296600-85312800 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
11 | chr1:85296800-85299000 | Weak transcription | NHEK | skin |
12 | chr1:85297000-85299400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |