Variant report

Variant rs17009072
Chromosome Location chr4:125963132-125963133
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:125960800-125963200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
2 chr4:125961600-125964200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr4:125961600-125964400 Enhancers NHEK skin
4 chr4:125961800-125964200 Enhancers HMEC breast
5 chr4:125962000-125963800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr4:125962000-125964000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr4:125962200-125965400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr4:125962400-125963200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr4:125962400-125963400 Weak transcription Placenta Amnion Placenta Amnion
10 chr4:125962600-125963600 Enhancers Fetal Heart heart

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