Variant report

Variant rs9493307
Chromosome Location chr6:132724620-132724621
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132723400-132725000 Weak transcription NHLF lung
2 chr6:132723400-132725200 Weak transcription NH-A brain
3 chr6:132723400-132725600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr6:132723400-132725800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr6:132723400-132726000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr6:132723400-132726000 Weak transcription HSMM muscle
7 chr6:132723400-132726600 Enhancers NHDF-Ad bronchial
8 chr6:132723600-132725400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr6:132724200-132727800 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr6:132724400-132725200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
11 chr6:132724400-132726400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr6:132724600-132724800 Bivalent Enhancer IMR90 fetal lung fibroblasts Cell Line lung
13 chr6:132724600-132724800 Flanking Active TSS Fetal Kidney kidney
14 chr6:132724600-132725000 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr6:132724600-132727000 Flanking Active TSS GM12878-XiMat blood

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