Variant report

Variant rs34168776
Chromosome Location chr11:16550508-16550509
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16544600-16558200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
2 chr11:16548400-16552400 Enhancers Skeletal Muscle Male skeletal muscle
3 chr11:16548600-16552400 Enhancers Skeletal Muscle Female skeletal muscle
4 chr11:16549200-16552000 Enhancers Pancreatic Islets Pancreatic Islet
5 chr11:16549400-16551000 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr11:16549400-16556200 Weak transcription Left Ventricle heart
7 chr11:16549600-16550600 Enhancers Psoas Muscle Psoas
8 chr11:16550000-16550600 Enhancers Adipose Nuclei Adipose
9 chr11:16550000-16550600 Enhancers Fetal Heart heart
10 chr11:16550000-16551400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr11:16550200-16550600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr11:16550400-16551000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr11:16550400-16551000 Enhancers Fetal Muscle Leg muscle

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