Variant report
Variant | rs57826478 |
---|---|
Chromosome Location | chr6:145586882-145586883 |
allele | A/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:145579400-145593600 | Weak transcription | Fetal Kidney | kidney |
2 | chr6:145584200-145587000 | Weak transcription | Fetal Intestine Small | intestine |
3 | chr6:145584200-145593200 | Weak transcription | Primary T helper memory cells from peripheral blood 1 | blood |
4 | chr6:145585400-145587600 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
5 | chr6:145585600-145587400 | Weak transcription | Fetal Brain Male | brain |
6 | chr6:145586000-145588000 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
7 | chr6:145586200-145587200 | Enhancers | HepG2 | liver |
8 | chr6:145586200-145588000 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
9 | chr6:145586800-145587200 | Enhancers | Adipose Nuclei | Adipose |
10 | chr6:145586800-145587800 | Enhancers | Fetal Intestine Large | intestine |
11 | chr6:145586800-145588800 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |