Variant report

Variant rs4719514
Chromosome Location chr7:17657690-17657691
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17641600-17663000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr7:17648800-17663200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr7:17653600-17663200 Weak transcription Aorta Aorta
4 chr7:17656800-17660200 Enhancers Hela-S3 cervix
5 chr7:17657000-17657800 Enhancers Fetal Intestine Large intestine
6 chr7:17657000-17658000 Enhancers Fetal Intestine Small intestine
7 chr7:17657400-17657800 Enhancers Gastric stomach
8 chr7:17657400-17657800 Enhancers Pancreas Pancrea
9 chr7:17657400-17658000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr7:17657400-17658000 Flanking Active TSS Liver Liver
11 chr7:17657400-17658000 Weak transcription Pancreatic Islets Pancreatic Islet
12 chr7:17657600-17657800 Enhancers Duodenum Mucosa Duodenum
13 chr7:17657600-17658200 Enhancers Stomach Mucosa stomach
14 chr7:17657600-17658200 Flanking Active TSS HepG2 liver

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