Variant report

Variant rs11226622
Chromosome Location chr11:105015470-105015471
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:105010600-105015600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr11:105010600-105015600 Weak transcription NHEK skin
3 chr11:105010600-105026400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr11:105013200-105016000 Enhancers HUVEC blood vessel
5 chr11:105015200-105016000 Enhancers HMEC breast
6 chr11:105015200-105016400 Enhancers NHLF lung
7 chr11:105015200-105016600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr11:105015400-105016000 Enhancers NH-A brain

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