Variant report

Variant rs7560083
Chromosome Location chr2:133868131-133868132
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:133854800-133892000 Weak transcription Left Ventricle heart
2 chr2:133865200-133870400 Weak transcription NHLF lung
3 chr2:133866600-133868400 Enhancers NHDF-Ad bronchial
4 chr2:133867200-133868400 Enhancers NHEK skin
5 chr2:133867600-133868400 Enhancers Brain Substantia Nigra brain
6 chr2:133867600-133868600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr2:133867800-133868200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr2:133867800-133868200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr2:133867800-133877000 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr2:133868000-133870400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr2:133868000-133885200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr2:133868000-133888200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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