Variant report

Variant rs12346978
Chromosome Location chr9:79058125-79058126
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
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 --

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