Variant report

Variant rs7866119
Chromosome Location chr9:7374793-7374794
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:7364400-7377000 Weak transcription Ovary ovary
2 chr9:7371000-7374800 Weak transcription HepG2 liver
3 chr9:7373800-7376000 Enhancers Fetal Stomach stomach
4 chr9:7373800-7380400 Enhancers Fetal Lung lung
5 chr9:7374200-7375600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
6 chr9:7374400-7375000 Enhancers Brain Substantia Nigra brain
7 chr9:7374400-7375000 Enhancers Pancreatic Islets Pancreatic Islet
8 chr9:7374400-7375400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr9:7374400-7375400 Enhancers Fetal Kidney kidney
10 chr9:7374400-7375600 Enhancers Fetal Muscle Leg muscle
11 chr9:7374600-7375600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung

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