Variant report

Variant rs10062004
Chromosome Location chr5:112694914-112694915
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:112682000-112700000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr5:112690200-112695400 Weak transcription HMEC breast
3 chr5:112690200-112700000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr5:112693200-112695400 Enhancers HUVEC blood vessel
5 chr5:112693400-112695200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
6 chr5:112693400-112695200 Enhancers Fetal Stomach stomach
7 chr5:112693400-112695200 Enhancers Stomach Mucosa stomach
8 chr5:112693600-112695000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr5:112693800-112695200 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr5:112694000-112695200 Enhancers Fetal Heart heart
11 chr5:112694000-112695800 Enhancers Colon Smooth Muscle Colon
12 chr5:112694200-112695800 Enhancers NH-A brain
13 chr5:112694800-112700000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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