Variant report

Variant rs35421306
Chromosome Location chr14:38166499-38166500
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:38153800-38166800 Weak transcription Liver Liver
2 chr14:38164800-38167200 Enhancers NH-A brain
3 chr14:38166200-38166600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr14:38166200-38167600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr14:38166200-38168400 Enhancers HepG2 liver
6 chr14:38166400-38166600 Enhancers A549 lung
7 chr14:38166400-38166800 Enhancers Hela-S3 cervix
8 chr14:38166400-38167200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr14:38166400-38167200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr14:38166400-38167200 Enhancers Muscle Satellite Cultured Cells --
11 chr14:38166400-38167200 Enhancers Stomach Mucosa stomach
12 chr14:38166400-38170000 Enhancers Fetal Intestine Large intestine

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