Variant report

Variant rs56223652
Chromosome Location chr4:8702483-8702484
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:8701600-8702600 Bivalent Enhancer Fetal Muscle Trunk muscle
2 chr4:8701600-8703400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr4:8702000-8702600 Bivalent/Poised TSS Stomach Smooth Muscle stomach
4 chr4:8702000-8702800 Bivalent Enhancer Fetal Stomach stomach
5 chr4:8702000-8703000 Bivalent Enhancer Fetal Lung lung
6 chr4:8702200-8702600 Flanking Bivalent TSS/Enh Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr4:8702200-8702600 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
8 chr4:8702200-8703600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr4:8702400-8702600 Bivalent Enhancer Adipose Nuclei Adipose
10 chr4:8702400-8702600 Bivalent Enhancer Fetal Brain Male brain
11 chr4:8702400-8702600 Enhancers Pancreas Pancrea
12 chr4:8702400-8702800 Flanking Bivalent TSS/Enh Breast Myoepithelial Primary Cells Breast
13 chr4:8702400-8702800 Bivalent Enhancer Fetal Muscle Leg muscle

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