Variant report

Variant rs544287651
Chromosome Location chr11:59962327-59962328
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 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 chr11:59961200-59962800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr11:59961200-59963600 Enhancers Fetal Intestine Small intestine
12 chr11:59961400-59962400 Enhancers Primary B cells from peripheral blood blood
13 chr11:59961400-59962400 Enhancers Primary hematopoietic stem cells short term culture blood
14 chr11:59961600-59962400 Enhancers HUES6 Cell Line embryonic stem cell
15 chr11:59961600-59963600 Enhancers Primary hematopoietic stem cells blood
16 chr11:59961600-59963600 Enhancers Ovary ovary
17 chr11:59961800-59962600 Flanking Active TSS K562 blood
18 chr11:59962000-59962400 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
19 chr11:59962000-59962400 Flanking Active TSS GM12878-XiMat blood
20 chr11:59962000-59962600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
21 chr11:59962200-59965000 Enhancers HUVEC blood vessel

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