Variant report

Variant rs11065538
Chromosome Location chr12:121816694-121816695
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:4 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:121815400-121820800 Weak transcription Fetal Intestine Small intestine
2 chr12:121816400-121817000 Enhancers HepG2 liver
3 chr12:121816600-121817000 Enhancers A549 lung
4 chr12:121816600-121817200 Enhancers Pancreatic Islets Pancreatic Islet

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