Variant report

Variant rs11029650
Chromosome Location chr11:26643635-26643636
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:26641600-26644800 Enhancers HMEC breast
2 chr11:26642000-26645000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr11:26642000-26645200 Enhancers NHEK skin
4 chr11:26642200-26643800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr11:26642200-26644800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr11:26642200-26644800 Enhancers NHDF-Ad bronchial
7 chr11:26642200-26645000 Enhancers Muscle Satellite Cultured Cells --
8 chr11:26642200-26645000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr11:26642200-26645000 Enhancers Placenta Amnion Placenta Amnion
10 chr11:26642200-26645200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr11:26642200-26645200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr11:26642200-26645200 Enhancers Hela-S3 cervix
13 chr11:26643000-26644400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
14 chr11:26643200-26644200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
15 chr11:26643600-26643800 Enhancers Fetal Intestine Small intestine
16 chr11:26643600-26644600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr11:26643600-26644800 Flanking Active TSS A549 lung

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