Variant report

Variant rs35692319
Chromosome Location chr7:18905701-18905702
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:18901600-18905800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
2 chr7:18903000-18940000 Weak transcription Aorta Aorta
3 chr7:18903800-18907400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr7:18904600-18906000 Enhancers Right Atrium heart
5 chr7:18904800-18907000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr7:18904800-18907400 Enhancers Adipose Nuclei Adipose
7 chr7:18905000-18907000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr7:18905200-18907000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr7:18905200-18908000 Enhancers NHDF-Ad bronchial
10 chr7:18905600-18906600 Enhancers Muscle Satellite Cultured Cells --
11 chr7:18905600-18907000 Enhancers NHLF lung
12 chr7:18905600-18907200 Enhancers Osteobl bone

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