Variant report

Variant rs7863039
Chromosome Location chr9:96764990-96764991
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:96759000-96767800 Weak transcription Pancreas Pancrea
2 chr9:96760200-96766000 Weak transcription Stomach Mucosa stomach
3 chr9:96762600-96768000 Weak transcription Fetal Intestine Large intestine
4 chr9:96763400-96767200 Weak transcription Gastric stomach
5 chr9:96764200-96765000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr9:96764200-96765000 Enhancers Stomach Smooth Muscle stomach
7 chr9:96764200-96765000 Enhancers Osteobl bone
8 chr9:96764400-96774200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr9:96764600-96765000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr9:96764600-96765000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
11 chr9:96764600-96765000 Enhancers Fetal Stomach stomach
12 chr9:96764800-96765000 Enhancers Liver Liver
13 chr9:96764800-96765000 Flanking Active TSS Sigmoid Colon Sigmoid Colon

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