Variant report

Variant rs73860652
Chromosome Location chr3:100184971-100184972
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100172200-100185200 Weak transcription Aorta Aorta
2 chr3:100183000-100185000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr3:100184400-100185600 Enhancers ES-I3 Cell Line embryonic stem cell
4 chr3:100184400-100186200 Enhancers Primary neutrophils fromperipheralblood blood
5 chr3:100184600-100185000 Enhancers Monocytes-CD14+_RO01746 blood
6 chr3:100184600-100185400 Enhancers NHEK skin
7 chr3:100184600-100185600 Flanking Active TSS GM12878-XiMat blood
8 chr3:100184600-100186200 Enhancers Primary monocytes fromperipheralblood blood
9 chr3:100184800-100185000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr3:100184800-100185200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr3:100184800-100185400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr3:100184800-100185400 Enhancers Liver Liver

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