Variant report

Variant rs180680432
Chromosome Location chr11:33423611-33423612
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:33413400-33466200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr11:33415400-33424800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr11:33415600-33434000 Weak transcription Fetal Brain Female brain
4 chr11:33420000-33425000 Weak transcription Brain Inferior Temporal Lobe brain
5 chr11:33423000-33423800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
6 chr11:33423200-33423800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr11:33423200-33424000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr11:33423400-33423800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr11:33423400-33424000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr11:33423400-33424000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
11 chr11:33423600-33423800 Enhancers Brain Germinal Matrix brain
12 chr11:33423600-33424400 Enhancers GM12878-XiMat blood

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