Variant report

Variant rs59509049
Chromosome Location chr2:190988968-190988969
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:190985000-190997200 Weak transcription Left Ventricle heart
2 chr2:190988200-190989400 Enhancers Placenta Placenta
3 chr2:190988400-190989000 Enhancers NH-A brain
4 chr2:190988400-190989200 Enhancers NHDF-Ad bronchial
5 chr2:190988400-190989200 Enhancers Osteobl bone
6 chr2:190988400-190989400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr2:190988400-190990000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr2:190988600-190989000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr2:190988800-190989000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr2:190988800-190989400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr2:190988800-190989400 Enhancers Fetal Intestine Large intestine

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