Variant report

Variant rs532900941
Chromosome Location chr4:1078739-1078740
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:1076800-1078800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
2 chr4:1076800-1080000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr4:1076800-1082400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr4:1078600-1078800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr4:1078600-1078800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
6 chr4:1078600-1079000 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin02 Skin
7 chr4:1078600-1080200 Enhancers Adipose Nuclei Adipose
8 chr4:1078600-1080200 Enhancers Pancreas Pancrea

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