Variant report

Variant rs17146058
Chromosome Location chr5:119424408-119424409
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:119423000-119425200 Enhancers Dnd41 blood
2 chr5:119423200-119428800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr5:119423600-119424800 Enhancers Primary T cells from cord blood blood
4 chr5:119423800-119425000 Enhancers Primary hematopoietic stem cells blood
5 chr5:119423800-119425000 Enhancers Monocytes-CD14+_RO01746 blood
6 chr5:119423800-119425200 Enhancers Primary neutrophils fromperipheralblood blood
7 chr5:119424000-119424800 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr5:119424000-119426800 Enhancers Fetal Heart heart
9 chr5:119424200-119424600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr5:119424200-119424600 Enhancers Primary monocytes fromperipheralblood blood
11 chr5:119424200-119424800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr5:119424400-119428600 Weak transcription Primary hematopoietic stem cells short term culture blood

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