Variant report

Variant rs17094828
Chromosome Location chr10:118247055-118247056
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:118238600-118249400 Weak transcription HMEC breast
2 chr10:118245800-118248200 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr10:118246200-118247400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr10:118246200-118248200 Enhancers Liver Liver
5 chr10:118246400-118247200 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr10:118246600-118247800 Enhancers Fetal Stomach stomach
7 chr10:118246600-118248000 Weak transcription Fetal Muscle Leg muscle
8 chr10:118246600-118248200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr10:118246600-118248400 Enhancers Adipose Nuclei Adipose
10 chr10:118246800-118247800 Weak transcription H9 Cell Line embryonic stem cell
11 chr10:118246800-118248800 Weak transcription HUES48 Cell Line embryonic stem cell
12 chr10:118247000-118247200 Enhancers Fetal Brain Male brain

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