Variant report

Variant rs73194463
Chromosome Location chr13:50431598-50431599
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:50422200-50436600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr13:50431000-50433000 Enhancers Muscle Satellite Cultured Cells --
3 chr13:50431200-50432400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr13:50431200-50433800 Enhancers NHLF lung
5 chr13:50431200-50434600 Enhancers HMEC breast
6 chr13:50431400-50431600 Enhancers Placenta Placenta
7 chr13:50431400-50431800 Flanking Active TSS A549 lung
8 chr13:50431400-50432400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr13:50431400-50432400 Flanking Active TSS HepG2 liver
10 chr13:50431400-50432800 Enhancers Pancreas Pancrea
11 chr13:50431400-50433600 Flanking Active TSS Liver Liver
12 chr13:50431400-50434000 Enhancers Hela-S3 cervix
13 chr13:50431400-50434000 Enhancers HSMM muscle
14 chr13:50431400-50434200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr13:50431400-50434200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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