Variant report

Variant rs9493193
Chromosome Location chr6:132469477-132469478
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132459600-132494800 Weak transcription Primary B cells from cord blood blood
2 chr6:132467200-132470000 Strong transcription HUVEC blood vessel
3 chr6:132467400-132470000 Enhancers NHDF-Ad bronchial
4 chr6:132467600-132471000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr6:132467800-132470000 Enhancers Osteobl bone
6 chr6:132467800-132470200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr6:132468000-132469800 Enhancers NHLF lung
8 chr6:132468000-132470000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr6:132468200-132469600 Enhancers Muscle Satellite Cultured Cells --
10 chr6:132468200-132469800 Enhancers Fetal Stomach stomach
11 chr6:132468200-132469800 Enhancers HSMMtube muscle
12 chr6:132468200-132469800 Enhancers NH-A brain
13 chr6:132468400-132470000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
14 chr6:132468600-132469600 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr6:132468600-132469600 Enhancers HSMM muscle
16 chr6:132468600-132470000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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