Variant report
Variant | rs16938995 |
---|---|
Chromosome Location | chr8:49780344-49780345 |
allele | A/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:49776800-49780600 | Weak transcription | Fetal Stomach | stomach |
2 | chr8:49776800-49782400 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
3 | chr8:49776800-49782400 | Weak transcription | Fetal Brain Female | brain |
4 | chr8:49778000-49781600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr8:49778400-49780800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
6 | chr8:49778400-49782400 | Weak transcription | Placenta Amnion | Placenta Amnion |
7 | chr8:49778600-49780600 | Weak transcription | NHEK | skin |
8 | chr8:49778600-49781800 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
9 | chr8:49779000-49781600 | Weak transcription | Fetal Brain Male | brain |
10 | chr8:49779000-49782400 | Weak transcription | Esophagus | oesophagus |
11 | chr8:49779200-49780400 | Weak transcription | Fetal Lung | lung |
12 | chr8:49779200-49780600 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
13 | chr8:49779200-49780600 | Weak transcription | HMEC | breast |
14 | chr8:49779200-49781800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
15 | chr8:49780200-49780800 | Enhancers | Ovary | ovary |
16 | chr8:49780200-49782400 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
17 | chr8:49780200-49782400 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
18 | chr8:49780200-49782400 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |