Variant report

Variant rs11205098
Chromosome Location chr1:152717432-152717433
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:152711600-152718600 Enhancers HMEC breast
2 chr1:152714200-152718600 Enhancers NHEK skin
3 chr1:152714400-152718200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr1:152714600-152721200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr1:152714800-152719200 Enhancers NHLF lung
6 chr1:152715200-152718600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:152715600-152718400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:152715800-152718600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr1:152715800-152720400 Enhancers NHDF-Ad bronchial
10 chr1:152716000-152718600 Enhancers Placenta Placenta
11 chr1:152717200-152718200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

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