Variant report

Variant rs11670025
Chromosome Location chr19:43491646-43491647
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43486200-43491800 Weak transcription NHLF lung
2 chr19:43490000-43492200 Weak transcription Osteobl bone
3 chr19:43490800-43494600 Enhancers NHEK skin
4 chr19:43491000-43492200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr19:43491000-43492200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr19:43491400-43491800 Enhancers Placenta Placenta
7 chr19:43491400-43492400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr19:43491600-43492600 Enhancers HMEC breast
9 chr19:43491600-43492600 Enhancers NHDF-Ad bronchial

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