Variant report

Variant rs11865391
Chromosome Location chr16:79845182-79845183
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:79843000-79847800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr16:79844000-79845200 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr16:79844000-79846400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr16:79844200-79845200 Enhancers iPS-20b Cell Line embryonic stem cell
5 chr16:79844200-79845800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr16:79844200-79846400 Enhancers HMEC breast
7 chr16:79844400-79845400 Flanking Active TSS NHEK skin
8 chr16:79844800-79845200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr16:79844800-79845400 Enhancers K562 blood
10 chr16:79844800-79846000 Enhancers Fetal Lung lung
11 chr16:79845000-79845200 Enhancers Esophagus oesophagus

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