Variant report

Variant rs11209392
Chromosome Location chr1:69587850-69587851
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:69586200-69588400 Enhancers Adipose Nuclei Adipose
2 chr1:69586200-69588600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr1:69586400-69592400 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr1:69586400-69596800 Weak transcription HUES48 Cell Line embryonic stem cell
5 chr1:69586600-69588000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
6 chr1:69586600-69588600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr1:69586600-69588600 Weak transcription Brain Hippocampus Middle brain
8 chr1:69586800-69592400 Weak transcription H1 Cell Line embryonic stem cell
9 chr1:69587000-69588000 Weak transcription Aorta Aorta
10 chr1:69587000-69592000 Weak transcription Fetal Brain Male brain
11 chr1:69587200-69588200 Enhancers HMEC breast
12 chr1:69587400-69588000 Enhancers NHEK skin
13 chr1:69587400-69588600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr1:69587400-69589400 Enhancers Brain Angular Gyrus brain
15 chr1:69587800-69588000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr1:69587800-69588200 Enhancers NHLF lung
17 chr1:69587800-69588800 Enhancers Colon Smooth Muscle Colon
18 chr1:69587800-69589000 Enhancers Stomach Smooth Muscle stomach

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