Variant report

Variant rs1384218
Chromosome Location chr8:49569981-49569982
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49563200-49572800 Weak transcription Pancreas Pancrea
2 chr8:49564400-49571200 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr8:49565000-49570200 Weak transcription Aorta Aorta
4 chr8:49567400-49575800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr8:49568600-49570200 Enhancers Fetal Lung lung
6 chr8:49569000-49570000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr8:49569200-49570000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr8:49569400-49570000 Enhancers H9 Cell Line embryonic stem cell
9 chr8:49569600-49570000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr8:49569600-49570000 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr8:49569600-49570200 Enhancers HUES64 Cell Line embryonic stem cell
12 chr8:49569800-49570000 Flanking Active TSS ES-I3 Cell Line embryonic stem cell
13 chr8:49569800-49570200 Enhancers HUES48 Cell Line embryonic stem cell
14 chr8:49569800-49570200 Enhancers iPS-20b Cell Line embryonic stem cell

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