Variant report

Variant rs34954743
Chromosome Location chr9:17799517-17799518
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:17787000-17800400 Weak transcription Fetal Brain Female brain
2 chr9:17788600-17805400 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr9:17796000-17812000 Weak transcription Aorta Aorta
4 chr9:17799000-17800600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr9:17799200-17800000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr9:17799400-17799600 Enhancers Fetal Brain Male brain
7 chr9:17799400-17799800 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr9:17799400-17799800 Enhancers Hela-S3 cervix
9 chr9:17799400-17800600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr9:17799400-17800600 Enhancers Fetal Heart heart

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