Variant report

Variant rs1539024
Chromosome Location chr10:45256614-45256615
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:45249200-45262400 Weak transcription Aorta Aorta
2 chr10:45249600-45265000 Weak transcription Gastric stomach
3 chr10:45256000-45257200 Enhancers Fetal Stomach stomach
4 chr10:45256400-45257000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr10:45256400-45257000 Enhancers Osteobl bone
6 chr10:45256400-45257400 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr10:45256600-45256800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr10:45256600-45257000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr10:45256600-45257000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr10:45256600-45257000 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
11 chr10:45256600-45257000 Enhancers Fetal Muscle Trunk muscle
12 chr10:45256600-45257000 Enhancers Fetal Muscle Leg muscle
13 chr10:45256600-45257000 Enhancers Ovary ovary
14 chr10:45256600-45257000 Enhancers Pancreas Pancrea
15 chr10:45256600-45257200 Enhancers Brain Germinal Matrix brain
16 chr10:45256600-45257200 Enhancers NH-A brain
17 chr10:45256600-45257200 Enhancers NHDF-Ad bronchial
18 chr10:45256600-45257400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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