Variant report

Variant rs373137668
Chromosome Location chr10:18279129-18279130
allele A/C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:18273600-18282000 Weak transcription Hela-S3 cervix
2 chr10:18276400-18280200 Enhancers GM12878-XiMat blood
3 chr10:18277400-18279800 Enhancers Primary B cells from peripheral blood blood
4 chr10:18277800-18283000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr10:18278000-18280200 Enhancers Primary B cells from cord blood blood
6 chr10:18278400-18280400 Enhancers NHDF-Ad bronchial
7 chr10:18278800-18279800 Enhancers NHLF lung
8 chr10:18278800-18280000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr10:18278800-18280200 Enhancers NHEK skin
10 chr10:18279000-18280000 Enhancers Muscle Satellite Cultured Cells --
11 chr10:18279000-18280000 Enhancers Osteobl bone
12 chr10:18279000-18280200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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