Variant report

Variant rs10897011
Chromosome Location chr11:59961427-59961428
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:59960200-59965000 Enhancers Primary monocytes fromperipheralblood blood
2 chr11:59960400-59962800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
3 chr11:59960400-59965400 Enhancers Dnd41 blood
4 chr11:59961000-59962400 Enhancers Primary neutrophils fromperipheralblood blood
5 chr11:59961000-59962400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr11:59961000-59962400 Enhancers HMEC breast
7 chr11:59961000-59963600 Enhancers Fetal Intestine Large intestine
8 chr11:59961000-59963800 Enhancers Primary B cells from cord blood blood
9 chr11:59961000-59965000 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr11:59961200-59962000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr11:59961200-59962800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr11:59961200-59963600 Enhancers Fetal Intestine Small intestine
13 chr11:59961400-59961600 Enhancers Primary T killer memory cells from peripheral blood blood
14 chr11:59961400-59961600 Flanking Active TSS GM12878-XiMat blood
15 chr11:59961400-59961600 Flanking Active TSS HUVEC blood vessel
16 chr11:59961400-59961600 Flanking Active TSS K562 blood
17 chr11:59961400-59962200 Enhancers HUES48 Cell Line embryonic stem cell
18 chr11:59961400-59962400 Enhancers Primary B cells from peripheral blood blood
19 chr11:59961400-59962400 Enhancers Primary hematopoietic stem cells short term culture blood

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