Variant report
Variant | rs10100701 |
---|---|
Chromosome Location | chr8:49625914-49625915 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:49612800-49626400 | Weak transcription | Placenta Amnion | Placenta Amnion |
2 | chr8:49618000-49626000 | Weak transcription | Fetal Kidney | kidney |
3 | chr8:49618200-49628000 | Weak transcription | Fetal Lung | lung |
4 | chr8:49619000-49626200 | Weak transcription | Spleen | Spleen |
5 | chr8:49621600-49628600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
6 | chr8:49622400-49628000 | Weak transcription | Ovary | ovary |
7 | chr8:49622800-49627400 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
8 | chr8:49622800-49627600 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
9 | chr8:49623000-49626000 | Enhancers | NHEK | skin |
10 | chr8:49624200-49627000 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
11 | chr8:49624400-49627000 | Enhancers | HMEC | breast |
12 | chr8:49624400-49627200 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
13 | chr8:49625600-49627000 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
14 | chr8:49625800-49626000 | Enhancers | Esophagus | oesophagus |
15 | chr8:49625800-49626200 | Flanking Active TSS | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
16 | chr8:49625800-49626800 | Enhancers | Placenta | Placenta |