Variant report

Variant rs17096690
Chromosome Location chr5:147582317-147582318
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:147573200-147584000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr5:147576600-147582400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr5:147579600-147583800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr5:147579800-147584800 Weak transcription Fetal Intestine Large intestine
5 chr5:147581400-147582400 Enhancers NHEK skin
6 chr5:147581600-147582800 Enhancers HMEC breast
7 chr5:147581600-147584800 Weak transcription Monocytes-CD14+_RO01746 blood
8 chr5:147581800-147584600 Weak transcription Primary monocytes fromperipheralblood blood
9 chr5:147582000-147582600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr5:147582200-147583400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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