Variant report

Variant rs60834821
Chromosome Location chr5:108340817-108340818
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:108301600-108361200 Weak transcription Primary T cells from cord blood blood
2 chr5:108328800-108342000 Weak transcription Right Atrium heart
3 chr5:108329600-108346200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr5:108329600-108359600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr5:108330200-108351800 Weak transcription Fetal Lung lung
6 chr5:108332600-108359400 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr5:108332800-108359800 Weak transcription Adipose Nuclei Adipose
8 chr5:108333400-108351600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr5:108334200-108341800 Weak transcription Esophagus oesophagus
10 chr5:108334200-108342000 Weak transcription Pancreas Pancrea
11 chr5:108334200-108342400 Weak transcription Skeletal Muscle Male skeletal muscle
12 chr5:108334200-108344200 Weak transcription Fetal Stomach stomach
13 chr5:108340400-108341000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr5:108340800-108341000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
15 chr5:108340800-108341200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr5:108340800-108341800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr5:108340800-108342200 Enhancers NHEK skin

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