Variant report

Variant rs11139651
Chromosome Location chr9:72273898-72273899
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:72253000-72285000 Weak transcription Fetal Brain Female brain
2 chr9:72253400-72274400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr9:72258200-72274000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr9:72260600-72286200 Weak transcription Aorta Aorta
5 chr9:72262400-72274200 Weak transcription Brain Angular Gyrus brain
6 chr9:72262600-72285400 Weak transcription Brain Cingulate Gyrus brain
7 chr9:72262800-72275600 Weak transcription Brain Hippocampus Middle brain
8 chr9:72264600-72275200 Weak transcription Fetal Stomach stomach
9 chr9:72269000-72274000 Weak transcription Ovary ovary
10 chr9:72272200-72276400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr9:72272600-72276000 Enhancers Liver Liver
12 chr9:72273000-72285600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
13 chr9:72273800-72274600 Enhancers Duodenum Smooth Muscle Duodenum
14 chr9:72273800-72275600 Enhancers Fetal Lung lung
15 chr9:72273800-72282600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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