Variant report

Variant rs374674339
Chromosome Location chr1:78758316-78758317
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr1:78757200-78758600 Enhancers Muscle Satellite Cultured Cells --
4 chr1:78757200-78758600 Enhancers HSMMtube muscle
5 chr1:78757600-78758400 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr1:78757600-78758400 Enhancers Fetal Muscle Leg muscle
7 chr1:78757800-78758400 Enhancers HSMM muscle
8 chr1:78758000-78758400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr1:78758000-78758400 Enhancers Osteobl bone
10 chr1:78758200-78758400 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
11 chr1:78758200-78758400 Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
12 chr1:78758200-78758400 Enhancers Pancreas Pancrea
13 chr1:78758200-78758600 ZNF genes & repeats Liver Liver
14 chr1:78758200-78759000 Enhancers NHDF-Ad bronchial

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