Variant report

Variant rs374309005
Chromosome Location chr4:1078970-1078971
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 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 chr4:1078600-1079000 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin02 Skin
4 chr4:1078600-1080200 Enhancers Adipose Nuclei Adipose
5 chr4:1078600-1080200 Enhancers Pancreas Pancrea
6 chr4:1078800-1079000 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr4:1078800-1079000 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin01 Skin
8 chr4:1078800-1079000 Bivalent Enhancer NHDF-Ad bronchial
9 chr4:1078800-1079200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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