Variant report

Variant rs10974743
Chromosome Location chr9:479507-479508
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr9:477800-481000 Enhancers Fetal Kidney kidney
8 chr9:478000-481400 Weak transcription Aorta Aorta
9 chr9:478200-484000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr9:479000-479800 Enhancers Placenta Placenta
11 chr9:479200-479600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr9:479200-479800 Enhancers HMEC breast
13 chr9:479400-480000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr9:479400-484400 Weak transcription H1 Cell Line embryonic stem cell

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