Variant report

Variant rs71453643
Chromosome Location chr14:35118046-35118047
allele -/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:35115600-35119200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr14:35117000-35121600 Enhancers Placenta Placenta
3 chr14:35117600-35118200 Enhancers A549 lung
4 chr14:35117600-35118200 Enhancers K562 blood
5 chr14:35117600-35120000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr14:35118000-35118200 Enhancers Muscle Satellite Cultured Cells --
7 chr14:35118000-35118200 Flanking Active TSS Hela-S3 cervix
8 chr14:35118000-35118200 Enhancers Osteobl bone
9 chr14:35118000-35118400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr14:35118000-35118400 Flanking Bivalent TSS/Enh HepG2 liver
11 chr14:35118000-35118400 Enhancers NH-A brain
12 chr14:35118000-35120600 Enhancers NHDF-Ad bronchial
13 chr14:35118000-35120800 Enhancers NHLF lung

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