Variant report

Variant rs11910896
Chromosome Location chr21:17489508-17489509
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:17485800-17489600 Weak transcription Rectal Smooth Muscle rectum
2 chr21:17488600-17489600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr21:17488600-17489800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
4 chr21:17488800-17489600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr21:17488800-17490600 Enhancers Fetal Kidney kidney
6 chr21:17489000-17490200 Flanking Active TSS Muscle Satellite Cultured Cells --
7 chr21:17489200-17490200 Flanking Active TSS A549 lung
8 chr21:17489200-17490600 Enhancers HSMM muscle
9 chr21:17489400-17489600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr21:17489400-17489600 Enhancers Brain Inferior Temporal Lobe brain
11 chr21:17489400-17489800 Flanking Active TSS Osteobl bone
12 chr21:17489400-17490000 Enhancers Adipose Nuclei Adipose
13 chr21:17489400-17490200 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr21:17489400-17490200 Flanking Active TSS NH-A brain
15 chr21:17489400-17490200 Flanking Active TSS NHDF-Ad bronchial
16 chr21:17489400-17490600 Active TSS Aorta Aorta
17 chr21:17489400-17490600 Flanking Active TSS HUVEC blood vessel
18 chr21:17489400-17490800 Enhancers Cortex derived primary cultured neurospheres brain

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