Variant report
Variant | rs16851589 |
---|---|
Chromosome Location | chr3:141369966-141369967 |
allele | A/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:141363200-141371400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr3:141364400-141377600 | Weak transcription | Aorta | Aorta |
3 | chr3:141366000-141372200 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
4 | chr3:141367600-141372200 | Weak transcription | Fetal Stomach | stomach |
5 | chr3:141367800-141370600 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
6 | chr3:141367800-141370800 | Weak transcription | Rectal Smooth Muscle | rectum |
7 | chr3:141369200-141371400 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
8 | chr3:141369600-141373400 | Enhancers | Colon Smooth Muscle | Colon |
9 | chr3:141369800-141370800 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
10 | chr3:141369800-141371600 | Enhancers | K562 | blood |