Variant report

Variant rs35875926
Chromosome Location chr5:178802000-178802001
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:178798600-178804000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
2 chr5:178799000-178804000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr5:178799200-178804000 Weak transcription Muscle Satellite Cultured Cells --
4 chr5:178801000-178802200 Weak transcription Osteobl bone
5 chr5:178801000-178802600 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
6 chr5:178801000-178803800 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr5:178801000-178804000 Weak transcription HSMMtube muscle
8 chr5:178801600-178802600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
9 chr5:178801800-178802200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr5:178801800-178802600 Enhancers Spleen Spleen
11 chr5:178802000-178802200 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
12 chr5:178802000-178802400 Bivalent Enhancer Fetal Stomach stomach

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