Variant report

Variant rs10053341
Chromosome Location chr5:112784007-112784008
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:112762000-112786000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr5:112764600-112786400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr5:112764800-112786800 Weak transcription NHEK skin
4 chr5:112770600-112786800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr5:112780400-112787400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr5:112782200-112789600 Enhancers Fetal Stomach stomach
7 chr5:112783200-112784200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr5:112783600-112784200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
9 chr5:112783600-112784200 Enhancers Fetal Lung lung
10 chr5:112783600-112785000 Enhancers Liver Liver
11 chr5:112783800-112786000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr5:112784000-112787800 Weak transcription Fetal Heart heart

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