Variant report

Variant rs1008939
Chromosome Location chr13:50385946-50385947
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr13:50384600-50386200 Enhancers Osteobl bone
6 chr13:50384600-50387200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr13:50384800-50386200 Enhancers Muscle Satellite Cultured Cells --
8 chr13:50384800-50389600 Weak transcription Placenta Placenta
9 chr13:50385000-50386000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr13:50385000-50386200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr13:50385000-50389400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr13:50385200-50386000 Flanking Active TSS HepG2 liver
13 chr13:50385400-50386600 Weak transcription Skeletal Muscle Female skeletal muscle
14 chr13:50385400-50387200 Weak transcription Fetal Lung lung
15 chr13:50385600-50386800 Weak transcription Skeletal Muscle Male skeletal muscle
16 chr13:50385600-50387200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
17 chr13:50385600-50387800 Weak transcription A549 lung
18 chr13:50385600-50388200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
19 chr13:50385800-50386000 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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