Variant report

Variant rs149831392
Chromosome Location chr5:179868661-179868662
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:179866000-179869800 Enhancers Placenta Placenta
2 chr5:179867400-179868800 Weak transcription Pancreas Pancrea
3 chr5:179867600-179868800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr5:179867600-179868800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr5:179867600-179869000 Enhancers HepG2 liver
6 chr5:179868400-179868800 Enhancers iPS-15b Cell Line embryonic stem cell
7 chr5:179868400-179869200 Enhancers H1 Cell Line embryonic stem cell
8 chr5:179868400-179869200 Flanking Active TSS Hela-S3 cervix
9 chr5:179868600-179869000 Bivalent/Poised TSS Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr5:179868600-179869000 Flanking Active TSS A549 lung
11 chr5:179868600-179869200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin

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