Variant report

Variant rs2399749
Chromosome Location chr11:93760614-93760615
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:93755800-93761200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr11:93758000-93760800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr11:93759400-93761400 Weak transcription NH-A brain
4 chr11:93760200-93761000 Genic enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr11:93760400-93764000 Enhancers HMEC breast
6 chr11:93760400-93764000 Enhancers NHEK skin
7 chr11:93760600-93760800 Enhancers Fetal Lung lung
8 chr11:93760600-93762200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr11:93760600-93763200 Enhancers Placenta Amnion Placenta Amnion

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