Variant report

Variant rs547477849
Chromosome Location chr17:59497326-59497327
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:59491000-59504200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr17:59494600-59503000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr17:59495600-59503400 Weak transcription NHLF lung
4 chr17:59497000-59497600 Enhancers HepG2 liver
5 chr17:59497200-59497400 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr17:59497200-59497400 Bivalent Enhancer Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr17:59497200-59497400 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr17:59497200-59497600 Enhancers Placenta Placenta
9 chr17:59497200-59498000 Enhancers Dnd41 blood
10 chr17:59497200-59498200 Bivalent Enhancer Fetal Muscle Leg muscle
11 chr17:59497200-59498600 Enhancers Fetal Lung lung

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