Variant report

Variant rs9808767
Chromosome Location chr21:17496673-17496674
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:17490800-17497000 Weak transcription Colon Smooth Muscle Colon
2 chr21:17494400-17497000 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr21:17494800-17497000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr21:17495800-17497000 Weak transcription Adipose Nuclei Adipose
5 chr21:17496000-17496800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr21:17496000-17496800 Enhancers NHDF-Ad bronchial
7 chr21:17496000-17497000 Enhancers Muscle Satellite Cultured Cells --
8 chr21:17496000-17497600 Enhancers Fetal Lung lung
9 chr21:17496000-17497800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr21:17496200-17496800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr21:17496200-17496800 Enhancers Hela-S3 cervix
12 chr21:17496200-17497000 Enhancers Osteobl bone
13 chr21:17496200-17497600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr21:17496200-17497600 Enhancers NH-A brain
15 chr21:17496200-17497800 Enhancers NHLF lung
16 chr21:17496600-17497400 Enhancers A549 lung
17 chr21:17496600-17497800 Enhancers NHEK skin

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