Variant report

Variant rs535947376
Chromosome Location chr1:78758657-78758658
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:78753000-78768800 Weak transcription NHLF lung
2 chr1:78754400-78759000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr1:78758200-78759000 Enhancers NHDF-Ad bronchial
4 chr1:78758400-78758800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr1:78758400-78759000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr1:78758400-78759000 Weak transcription Fetal Muscle Leg muscle
7 chr1:78758400-78768800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr1:78758400-78769400 Weak transcription Pancreas Pancrea
9 chr1:78758600-78759400 Weak transcription Liver Liver

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