Variant report

Variant rs73437600
Chromosome Location chr11:26212082-26212083
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:26210200-26212400 Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
2 chr11:26210200-26212600 Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
3 chr11:26210400-26214200 Weak transcription Placenta Placenta
4 chr11:26210800-26212200 Active TSS Adipose Nuclei Adipose
5 chr11:26210800-26212400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr11:26211000-26216200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr11:26211200-26216600 Weak transcription Fetal Kidney kidney
8 chr11:26211600-26212400 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr11:26211600-26214800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr11:26211600-26216800 Weak transcription Osteobl bone
11 chr11:26211600-26220600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr11:26211800-26212200 Enhancers NHDF-Ad bronchial
13 chr11:26211800-26212800 Weak transcription Fetal Lung lung
14 chr11:26211800-26220200 Weak transcription NHLF lung
15 chr11:26212000-26212200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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