Variant report

Variant rs16932585
Chromosome Location chr11:16148799-16148800
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16145800-16149200 Enhancers HepG2 liver
2 chr11:16146400-16149400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr11:16147000-16149200 Enhancers Pancreatic Islets Pancreatic Islet
4 chr11:16147600-16149400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr11:16147600-16149400 Enhancers Fetal Lung lung
6 chr11:16147600-16149800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr11:16148400-16155600 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr11:16148400-16160200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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