Variant report

Variant rs11238709
Chromosome Location chr10:44289699-44289700
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:44277800-44295000 Weak transcription Spleen Spleen
2 chr10:44286000-44302600 Weak transcription Aorta Aorta
3 chr10:44286800-44292400 Weak transcription Ovary ovary
4 chr10:44287600-44290000 Enhancers Fetal Lung lung
5 chr10:44288600-44290200 Enhancers Fetal Muscle Leg muscle
6 chr10:44289000-44289800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr10:44289000-44290000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr10:44289000-44290000 Enhancers NHDF-Ad bronchial
9 chr10:44289000-44290200 Enhancers Adipose Nuclei Adipose
10 chr10:44289000-44290800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr10:44289000-44290800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr10:44289200-44289800 Enhancers Primary monocytes fromperipheralblood blood
13 chr10:44289200-44289800 Enhancers NHLF lung
14 chr10:44289200-44290000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
15 chr10:44289400-44290000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
16 chr10:44289400-44290000 Enhancers Fetal Stomach stomach
17 chr10:44289600-44289800 Bivalent Enhancer Liver Liver
18 chr10:44289600-44290000 Enhancers Right Atrium heart
19 chr10:44289600-44290000 Enhancers Osteobl bone
20 chr10:44289600-44290200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin

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