Variant report

Variant rs7803926
Chromosome Location chr7:17658420-17658421
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr7:17657800-17658600 Enhancers Placenta Placenta
6 chr7:17657800-17658600 Active TSS Rectal Mucosa Donor 29 rectum
7 chr7:17657800-17658600 Active TSS Rectal Mucosa Donor 31 rectum
8 chr7:17658000-17658600 Active TSS Liver Liver
9 chr7:17658000-17658800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr7:17658200-17658600 Weak transcription Stomach Mucosa stomach
11 chr7:17658200-17658600 Active TSS HepG2 liver
12 chr7:17658200-17658800 Active TSS Fetal Intestine Small intestine
13 chr7:17658400-17658600 Flanking Active TSS Duodenum Mucosa Duodenum
14 chr7:17658400-17658600 Flanking Active TSS Pancreatic Islets Pancreatic Islet
15 chr7:17658400-17659200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
16 chr7:17658400-17659400 Enhancers Fetal Intestine Large intestine

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