Variant report

Variant rs3758946
Chromosome Location chr11:18270898-18270899
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:18260000-18278200 Weak transcription Aorta Aorta
2 chr11:18268600-18276000 Weak transcription Esophagus oesophagus
3 chr11:18270200-18271000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr11:18270200-18271200 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr11:18270200-18273200 Enhancers GM12878-XiMat blood
6 chr11:18270600-18271000 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr11:18270800-18271000 Flanking Active TSS H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr11:18270800-18274600 Weak transcription Adipose Nuclei Adipose

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