Variant report

Variant rs1503792
Chromosome Location chr1:242641126-242641127
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:242616200-242651400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr1:242640400-242641200 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr1:242640800-242641400 Enhancers Fetal Lung lung
4 chr1:242640800-242641800 Enhancers Fetal Adrenal Gland Adrenal Gland
5 chr1:242640800-242641800 Enhancers Right Ventricle heart
6 chr1:242641000-242641800 Enhancers Aorta Aorta
7 chr1:242641000-242644400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr1:242641000-242653200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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