Variant report
Variant | rs12346978 |
---|---|
Chromosome Location | chr9:79058125-79058126 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:79057200-79058800 | Weak transcription | HepG2 | liver |
2 | chr9:79057200-79059200 | Weak transcription | Primary T regulatory cells fromperipheralblood | blood |
3 | chr9:79057200-79062200 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
4 | chr9:79057200-79062600 | Weak transcription | Primary T helper memory cells from peripheral blood 2 | blood |
5 | chr9:79057400-79062600 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
6 | chr9:79057400-79062600 | Weak transcription | Muscle Satellite Cultured Cells | -- |
7 | chr9:79057400-79062600 | Weak transcription | Osteobl | bone |
8 | chr9:79057800-79058200 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
9 | chr9:79057800-79058200 | ZNF genes & repeats | Fetal Intestine Small | intestine |
10 | chr9:79058000-79059000 | Weak transcription | GM12878-XiMat | blood |
11 | chr9:79058000-79062800 | Weak transcription | Primary T helper 17 cells PMA-I stimulated | -- |