Variant report

Variant rs17159621
Chromosome Location chr5:106589749-106589750
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:106586200-106590600 Enhancers Fetal Lung lung
2 chr5:106586800-106590200 Weak transcription Fetal Kidney kidney
3 chr5:106587200-106591000 Enhancers Fetal Stomach stomach
4 chr5:106588400-106590400 Enhancers Osteobl bone
5 chr5:106588400-106591200 Enhancers Primary Natural Killer cells fromperipheralblood blood
6 chr5:106588800-106590400 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr5:106589000-106589800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
8 chr5:106589000-106590000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr5:106589000-106590200 Enhancers Skeletal Muscle Male skeletal muscle
10 chr5:106589000-106590400 Enhancers Aorta Aorta
11 chr5:106589000-106590400 Enhancers Colon Smooth Muscle Colon
12 chr5:106589000-106590400 Enhancers Skeletal Muscle Female skeletal muscle
13 chr5:106589000-106590600 Enhancers HSMMtube muscle
14 chr5:106589000-106591000 Enhancers Fetal Muscle Leg muscle
15 chr5:106589200-106590000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
16 chr5:106589200-106590400 Enhancers Cortex derived primary cultured neurospheres brain
17 chr5:106589200-106590600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
18 chr5:106589200-106590600 Enhancers Fetal Heart heart
19 chr5:106589600-106589800 Flanking Active TSS Stomach Smooth Muscle stomach

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