Variant report

Variant rs581818
Chromosome Location chr11:59951065-59951066
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:59946800-59952000 Active TSS Adipose Nuclei Adipose
2 chr11:59947600-59953000 Enhancers Fetal Intestine Small intestine
3 chr11:59949800-59952000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr11:59950000-59951600 Enhancers HUVEC blood vessel
5 chr11:59950000-59954800 Enhancers Primary B cells from peripheral blood blood
6 chr11:59950200-59951400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr11:59950200-59951400 Weak transcription Spleen Spleen
8 chr11:59950400-59952600 Enhancers Primary hematopoietic stem cells blood
9 chr11:59950400-59954600 Enhancers Fetal Intestine Large intestine
10 chr11:59950600-59951400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
11 chr11:59950600-59951400 Weak transcription K562 blood
12 chr11:59950600-59951600 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr11:59950600-59951800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr11:59950600-59951800 Weak transcription Liver Liver
15 chr11:59950600-59954600 Flanking Active TSS Monocytes-CD14+_RO01746 blood
16 chr11:59950800-59951200 Enhancers Primary neutrophils fromperipheralblood blood
17 chr11:59950800-59951600 Enhancers Primary hematopoietic stem cells short term culture blood
18 chr11:59950800-59961200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
19 chr11:59951000-59951600 Flanking Active TSS Primary monocytes fromperipheralblood blood
20 chr11:59951000-59954200 Enhancers GM12878-XiMat blood
21 chr11:59951000-59954600 Enhancers Primary B cells from cord blood blood

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