Variant report

Variant rs3786547
Chromosome Location chr19:41506191-41506192
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:41505600-41506200 Enhancers Stomach Mucosa stomach
2 chr19:41505600-41508000 Genic enhancers Liver Liver
3 chr19:41505600-41509400 Enhancers Fetal Intestine Small intestine
4 chr19:41505800-41506400 Enhancers Duodenum Mucosa Duodenum
5 chr19:41505800-41506400 Flanking Active TSS A549 lung
6 chr19:41505800-41506600 Enhancers HMEC breast
7 chr19:41505800-41507400 Enhancers Fetal Intestine Large intestine
8 chr19:41506000-41506200 Bivalent Enhancer Small Intestine intestine
9 chr19:41506000-41506400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr19:41506000-41506400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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