Variant report

Variant rs61879669
Chromosome Location chr11:17070527-17070528
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:17066800-17070600 Enhancers Fetal Intestine Small intestine
2 chr11:17067400-17071000 Enhancers Fetal Intestine Large intestine
3 chr11:17067600-17071000 Enhancers HepG2 liver
4 chr11:17069400-17096200 Weak transcription Pancreas Pancrea
5 chr11:17069600-17070600 Enhancers Placenta Placenta
6 chr11:17069800-17071000 Enhancers A549 lung

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