Variant report

Variant rs7802758
Chromosome Location chr7:4120760-4120761
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:4088800-4129400 Weak transcription Right Ventricle heart
2 chr7:4103000-4125600 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr7:4109600-4122000 Weak transcription Esophagus oesophagus
4 chr7:4110200-4129400 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr7:4112400-4130200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr7:4113800-4120800 Weak transcription H1 Cell Line embryonic stem cell
7 chr7:4116200-4129200 Weak transcription Duodenum Smooth Muscle Duodenum
8 chr7:4117800-4129400 Weak transcription Fetal Intestine Small intestine
9 chr7:4118000-4128600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr7:4118800-4128400 Weak transcription Aorta Aorta
11 chr7:4119400-4121600 Weak transcription Spleen Spleen
12 chr7:4119400-4153000 Weak transcription Gastric stomach
13 chr7:4119600-4125800 Weak transcription Fetal Stomach stomach
14 chr7:4119800-4125800 Weak transcription Pancreas Pancrea
15 chr7:4120000-4120800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
16 chr7:4120200-4129000 Weak transcription Cortex derived primary cultured neurospheres brain
17 chr7:4120600-4121000 Strong transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
18 chr7:4120600-4121200 Enhancers Fetal Brain Male brain

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