Variant report

Variant rs59826931
Chromosome Location chr2:190145792-190145793
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:190141000-190149600 Weak transcription HSMM muscle
2 chr2:190141200-190150200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:190142200-190149400 Weak transcription NHDF-Ad bronchial
4 chr2:190142800-190149400 Weak transcription Osteobl bone
5 chr2:190142800-190149600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr2:190143000-190145800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr2:190143400-190149400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr2:190145400-190146600 Enhancers Fetal Lung lung
9 chr2:190145600-190146200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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