Variant report

Variant rs17226557
Chromosome Location chr20:13286416-13286417
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:13276800-13294200 Weak transcription iPS-15b Cell Line embryonic stem cell
2 chr20:13281000-13287400 Weak transcription Liver Liver
3 chr20:13284400-13287400 Weak transcription Fetal Intestine Large intestine
4 chr20:13284600-13287600 Weak transcription HepG2 liver
5 chr20:13285000-13293800 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr20:13286000-13287600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr20:13286200-13287000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr20:13286400-13286800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr20:13286400-13287600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr20:13286400-13288800 Enhancers Fetal Intestine Small intestine

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