Variant report

Variant rs17774276
Chromosome Location chr20:14615222-14615223
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14612600-14615400 Weak transcription Fetal Intestine Small intestine
2 chr20:14613600-14615800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr20:14614200-14616200 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr20:14614200-14616200 Enhancers HMEC breast
5 chr20:14614400-14615800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr20:14614400-14616200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr20:14614400-14616200 Enhancers NHEK skin
8 chr20:14614600-14615800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr20:14614600-14616000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr20:14614600-14616000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr20:14615000-14616200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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