Variant report

Variant rs16935397
Chromosome Location chr9:17186374-17186375
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:17159800-17195600 Weak transcription Aorta Aorta
2 chr9:17172200-17193600 Weak transcription Pancreas Pancrea
3 chr9:17174000-17188200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr9:17179000-17204400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr9:17185600-17186600 Enhancers Cortex derived primary cultured neurospheres brain
6 chr9:17185800-17191200 Weak transcription Fetal Heart heart
7 chr9:17186000-17190600 Weak transcription Fetal Lung lung
8 chr9:17186200-17186400 Enhancers Brain Germinal Matrix brain

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