Variant report
Variant | rs73981061 |
---|---|
Chromosome Location | chr2:191202978-191202979 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:191191600-191208000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr2:191198400-191207400 | Weak transcription | Spleen | Spleen |
3 | chr2:191198400-191207600 | Weak transcription | NHLF | lung |
4 | chr2:191198600-191208000 | Weak transcription | Aorta | Aorta |
5 | chr2:191198800-191208000 | Weak transcription | Ovary | ovary |
6 | chr2:191199600-191205000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
7 | chr2:191199600-191207600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
8 | chr2:191199600-191208000 | Weak transcription | HMEC | breast |
9 | chr2:191200200-191204400 | Weak transcription | A549 | lung |
10 | chr2:191200600-191208000 | Weak transcription | Left Ventricle | heart |
11 | chr2:191200800-191203000 | Weak transcription | Pancreas | Pancrea |
12 | chr2:191200800-191204000 | Weak transcription | Liver | Liver |
13 | chr2:191200800-191205200 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
14 | chr2:191200800-191207200 | Weak transcription | Fetal Intestine Small | intestine |
15 | chr2:191200800-191207400 | Weak transcription | Stomach Mucosa | stomach |
16 | chr2:191201000-191205000 | Weak transcription | K562 | blood |
17 | chr2:191202000-191203200 | Enhancers | HepG2 | liver |