Variant report

Variant rs2282038
Chromosome Location chr9:478530-478531
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:471400-480000 Weak transcription Brain Substantia Nigra brain
2 chr9:471600-486000 Weak transcription A549 lung
3 chr9:472400-479800 Weak transcription Esophagus oesophagus
4 chr9:473200-480600 Weak transcription Pancreas Pancrea
5 chr9:475400-484000 Weak transcription Fetal Intestine Small intestine
6 chr9:476800-481200 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr9:477600-478600 Enhancers Placenta Placenta
8 chr9:477800-481000 Enhancers Fetal Kidney kidney
9 chr9:478000-478800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr9:478000-481400 Weak transcription Aorta Aorta
11 chr9:478200-479200 Weak transcription H1 Cell Line embryonic stem cell
12 chr9:478200-479200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr9:478200-484000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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