Variant report

Variant rs59091471
Chromosome Location chr15:39223839-39223840
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:39222600-39224000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr15:39222600-39225400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
3 chr15:39222600-39225400 Enhancers Muscle Satellite Cultured Cells --
4 chr15:39222600-39225600 Enhancers HSMM muscle
5 chr15:39222800-39224000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr15:39222800-39225200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr15:39223000-39224400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr15:39223000-39225600 Enhancers Osteobl bone
9 chr15:39223600-39224200 Enhancers NHLF lung
10 chr15:39223600-39224400 Enhancers Placenta Placenta
11 chr15:39223600-39225200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr15:39223800-39224000 Enhancers NHDF-Ad bronchial
13 chr15:39223800-39224800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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