Variant report

Variant rs536913810
Chromosome Location chr4:1079091-1079092
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:1076800-1080000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
2 chr4:1076800-1082400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr4:1078600-1080200 Enhancers Adipose Nuclei Adipose
4 chr4:1078600-1080200 Enhancers Pancreas Pancrea
5 chr4:1078800-1079200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr4:1079000-1079400 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
7 chr4:1079000-1080200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin

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