Variant report
Variant | rs13242576 |
---|---|
Chromosome Location | chr7:139897310-139897311 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:139888600-139905000 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
2 | chr7:139893000-139900000 | Weak transcription | Esophagus | oesophagus |
3 | chr7:139895400-139900200 | Weak transcription | Rectal Mucosa Donor 29 | rectum |
4 | chr7:139896400-139897400 | Enhancers | Placenta | Placenta |
5 | chr7:139896400-139897600 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
6 | chr7:139896400-139897600 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
7 | chr7:139896600-139897600 | Enhancers | HMEC | breast |
8 | chr7:139896600-139898000 | Enhancers | NHEK | skin |
9 | chr7:139896600-139898600 | Enhancers | HepG2 | liver |
10 | chr7:139896600-139899200 | Weak transcription | Osteobl | bone |
11 | chr7:139896800-139897600 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
12 | chr7:139897000-139898800 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
13 | chr7:139897000-139899200 | Weak transcription | K562 | blood |
14 | chr7:139897000-139900000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |