The 2.0 version of rSNPBase

Variant report

Variant rs58901177
Chromosome Location chr10:45848299-45848300
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:45847400-45848600 Weak transcription Primary T killer memory cells from peripheral blood blood
2 chr10:45847400-45850000 Enhancers Primary B cells from peripheral blood blood
3 chr10:45848000-45848800 Enhancers Primary T helper 17 cells PMA-I stimulated --
4 chr10:45848000-45848800 Flanking Active TSS GM12878-XiMat blood
5 chr10:45848200-45848400 Enhancers Primary B cells from cord blood blood
6 chr10:45848200-45848600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr10:45848200-45848600 Enhancers Primary mononuclear cells fromperipheralblood Blood
8 chr10:45848200-45848800 Bivalent Enhancer Esophagus oesophagus
9 chr10:45848200-45848800 Flanking Active TSS K562 blood
10 chr10:45848200-45849000 Enhancers Primary T helper memory cells from peripheral blood 2 blood
11 chr10:45848200-45850200 Enhancers Monocytes-CD14+_RO01746 blood
12 chr10:45848200-45850400 Enhancers Primary monocytes fromperipheralblood blood
13 chr10:45848200-45850400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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Last update: Aug 31, 2015