Variant report

Variant rs35991466
Chromosome Location chr1:152878006-152878007
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:152876000-152878200 Weak transcription Esophagus oesophagus
2 chr1:152876400-152878600 Enhancers HMEC breast
3 chr1:152876400-152882600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:152876600-152878200 Enhancers NHEK skin
5 chr1:152876600-152878400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr1:152876600-152880800 Enhancers GM12878-XiMat blood
7 chr1:152876600-152881800 Enhancers Placenta Amnion Placenta Amnion
8 chr1:152876800-152878600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr1:152877200-152878200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr1:152877200-152879600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr1:152877400-152878200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr1:152877400-152879600 Enhancers Muscle Satellite Cultured Cells --
13 chr1:152877600-152878200 Enhancers NHDF-Ad bronchial
14 chr1:152877600-152879200 Enhancers Primary Natural Killer cells fromperipheralblood blood
15 chr1:152877600-152879600 Enhancers NHLF lung
16 chr1:152877800-152879200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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