Variant report

Variant rs56798890
Chromosome Location chr2:133867729-133867730
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:133854800-133892000 Weak transcription Left Ventricle heart
2 chr2:133855600-133867800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr2:133865000-133867800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:133865200-133870400 Weak transcription NHLF lung
5 chr2:133866600-133868000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr2:133866600-133868400 Enhancers NHDF-Ad bronchial
7 chr2:133867200-133868000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr2:133867200-133868000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr2:133867200-133868400 Enhancers NHEK skin
10 chr2:133867400-133867800 Enhancers HMEC breast
11 chr2:133867400-133868000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr2:133867400-133868000 Enhancers Brain Hippocampus Middle brain
13 chr2:133867600-133868000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr2:133867600-133868400 Enhancers Brain Substantia Nigra brain
15 chr2:133867600-133868600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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