Variant report
Variant | rs61391568 |
---|---|
Chromosome Location | chr14:81074518-81074519 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:81062200-81082200 | Weak transcription | Dnd41 | blood |
2 | chr14:81072200-81075800 | Weak transcription | Ovary | ovary |
3 | chr14:81072200-81075800 | Weak transcription | NHLF | lung |
4 | chr14:81072600-81074800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
5 | chr14:81073000-81075200 | Weak transcription | A549 | lung |
6 | chr14:81073200-81074800 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
7 | chr14:81073400-81075800 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
8 | chr14:81073800-81076000 | Enhancers | Stomach Mucosa | stomach |
9 | chr14:81074200-81075200 | Enhancers | Pancreas | Pancrea |
10 | chr14:81074200-81076000 | Enhancers | Gastric | stomach |