Variant report

Variant rs13016849
Chromosome Location chr2:172986343-172986344
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:172983400-172986400 Enhancers HepG2 liver
2 chr2:172983400-172986600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
3 chr2:172983400-172986800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:172983400-172987600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr2:172984000-172987400 Enhancers HMEC breast
6 chr2:172985400-172986400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr2:172985800-172986600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr2:172985800-172986600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr2:172986000-172986800 Enhancers NHDF-Ad bronchial
10 chr2:172986200-172986400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
11 chr2:172986200-172986600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr2:172986200-172986600 Enhancers Osteobl bone
13 chr2:172986200-172986800 Enhancers Muscle Satellite Cultured Cells --
14 chr2:172986200-172986800 Flanking Active TSS NHEK skin

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