Variant report

Variant rs181405460
Chromosome Location chr18:30487249-30487250
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:30485400-30487600 Enhancers Fetal Brain Male brain
2 chr18:30485600-30489200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr18:30485800-30489800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr18:30486600-30488000 Enhancers Primary B cells from peripheral blood blood
5 chr18:30486800-30487400 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr18:30487000-30487600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr18:30487000-30487800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr18:30487000-30490400 Weak transcription HMEC breast
9 chr18:30487200-30487600 Enhancers Brain Hippocampus Middle brain
10 chr18:30487200-30490400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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