Variant report

Variant rs11648959
Chromosome Location chr16:77096269-77096270
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:77091200-77097800 Enhancers Primary neutrophils fromperipheralblood blood
2 chr16:77095200-77096400 Weak transcription Primary T cells from cord blood blood
3 chr16:77096000-77098000 Enhancers Brain Germinal Matrix brain
4 chr16:77096000-77098200 Enhancers Fetal Lung lung
5 chr16:77096200-77097400 Enhancers Fetal Kidney kidney
6 chr16:77096200-77098400 Enhancers Fetal Stomach stomach
7 chr16:77096200-77101400 Enhancers Fetal Adrenal Gland Adrenal Gland

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