Variant report

Variant rs55680751
Chromosome Location chr11:71891309-71891310
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:71886000-71892600 Weak transcription Primary neutrophils fromperipheralblood blood
2 chr11:71888200-71895800 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr11:71889600-71892600 Weak transcription Fetal Intestine Large intestine
4 chr11:71889600-71900200 Weak transcription Fetal Intestine Small intestine
5 chr11:71890400-71891600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr11:71890400-71892000 Weak transcription Right Ventricle heart
7 chr11:71890600-71891800 Enhancers NHEK skin
8 chr11:71890800-71892000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr11:71890800-71895400 Enhancers HMEC breast
10 chr11:71891000-71893400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr11:71891200-71891600 Weak transcription Hela-S3 cervix
12 chr11:71891200-71891800 Enhancers GM12878-XiMat blood
13 chr11:71891200-71892200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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