Variant report

Variant rs7722421
Chromosome Location chr5:112770845-112770846
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:112762000-112786000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr5:112764400-112779200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr5:112764600-112786400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr5:112764800-112786800 Weak transcription NHEK skin
5 chr5:112770200-112771200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr5:112770200-112773800 Enhancers Fetal Stomach stomach
7 chr5:112770400-112771000 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr5:112770400-112772200 Enhancers Fetal Muscle Leg muscle
9 chr5:112770400-112783400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr5:112770600-112771800 Enhancers Right Ventricle heart
11 chr5:112770600-112772000 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr5:112770600-112773600 Enhancers Fetal Heart heart
13 chr5:112770600-112786800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr5:112770800-112772000 Enhancers Right Atrium heart
15 chr5:112770800-112773000 Enhancers Fetal Brain Male brain
16 chr5:112770800-112773600 Enhancers Fetal Lung lung

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