Variant report

Variant rs4942871
Chromosome Location chr13:50385349-50385350
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:50383200-50387200 Enhancers Fetal Intestine Small intestine
2 chr13:50383600-50389400 Enhancers Fetal Heart heart
3 chr13:50384200-50390200 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr13:50384400-50387400 Enhancers Fetal Intestine Large intestine
5 chr13:50384600-50385600 Enhancers Ovary ovary
6 chr13:50384600-50386200 Enhancers Osteobl bone
7 chr13:50384600-50387200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr13:50384800-50385600 Enhancers A549 lung
9 chr13:50384800-50386200 Enhancers Muscle Satellite Cultured Cells --
10 chr13:50384800-50389600 Weak transcription Placenta Placenta
11 chr13:50385000-50385400 Enhancers Fetal Lung lung
12 chr13:50385000-50386000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr13:50385000-50386200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr13:50385000-50389400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr13:50385200-50385400 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr13:50385200-50385400 Enhancers Skeletal Muscle Male skeletal muscle
17 chr13:50385200-50385400 Enhancers Skeletal Muscle Female skeletal muscle
18 chr13:50385200-50385600 Flanking Active TSS IMR90 fetal lung fibroblasts Cell Line lung
19 chr13:50385200-50385600 Enhancers Pancreas Pancrea
20 chr13:50385200-50386000 Flanking Active TSS HepG2 liver

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