Variant report

Variant rs16834665
Chromosome Location chr1:192669073-192669074
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:192666800-192669400 Enhancers HepG2 liver
2 chr1:192667600-192673000 Enhancers Primary neutrophils fromperipheralblood blood
3 chr1:192668200-192669600 Enhancers A549 lung
4 chr1:192668400-192670800 Weak transcription Placenta Placenta
5 chr1:192669000-192669800 Enhancers NH-A brain
6 chr1:192669000-192671400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr1:192669000-192672000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr1:192669000-192672000 Enhancers Hela-S3 cervix
9 chr1:192669000-192673200 Enhancers NHLF lung

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