Variant report

Variant rs533309459
Chromosome Location chr2:37948253-37948254
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:37941800-37948400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr2:37946800-37949000 Enhancers Muscle Satellite Cultured Cells --
3 chr2:37947200-37948800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr2:37947200-37949800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
5 chr2:37947400-37949000 Enhancers Osteobl bone
6 chr2:37947600-37948400 Flanking Active TSS NHDF-Ad bronchial
7 chr2:37947600-37948600 Enhancers Fetal Thymus thymus
8 chr2:37947600-37948800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr2:37947600-37948800 Enhancers Fetal Brain Female brain
10 chr2:37947600-37949000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr2:37947800-37948600 Enhancers Primary monocytes fromperipheralblood blood
12 chr2:37947800-37948600 Enhancers Aorta Aorta
13 chr2:37947800-37948600 Enhancers Stomach Smooth Muscle stomach
14 chr2:37947800-37949000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr2:37947800-37949000 Enhancers NHLF lung
16 chr2:37948000-37948600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr2:37948200-37948600 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin

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