Variant report

Variant rs549169933
Chromosome Location chr14:96934615-96934616
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:96917200-96954800 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr14:96929400-96946200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr14:96929600-96935000 Weak transcription Stomach Mucosa stomach
4 chr14:96929600-96941600 Weak transcription Pancreas Pancrea
5 chr14:96932000-96935600 Enhancers Fetal Intestine Large intestine
6 chr14:96932800-96935800 Enhancers Fetal Intestine Small intestine
7 chr14:96932800-96936000 Enhancers Liver Liver
8 chr14:96934200-96935800 Enhancers Placenta Placenta
9 chr14:96934600-96935600 Enhancers Duodenum Mucosa Duodenum
10 chr14:96934600-96935600 Flanking Active TSS HepG2 liver

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