Variant report

Variant rs180919749
Chromosome Location chr11:71928659-71928660
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:71927400-71929600 Enhancers K562 blood
2 chr11:71927400-71930400 Enhancers Primary monocytes fromperipheralblood blood
3 chr11:71927600-71929800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
4 chr11:71927600-71930000 Enhancers Primary B cells from peripheral blood blood
5 chr11:71927800-71929400 Active TSS Adipose Nuclei Adipose
6 chr11:71927800-71929600 Bivalent/Poised TSS Fetal Muscle Leg muscle
7 chr11:71927800-71929800 Enhancers Primary B cells from cord blood blood
8 chr11:71927800-71930000 Enhancers Primary Natural Killer cells fromperipheralblood blood
9 chr11:71927800-71930000 Active TSS Placenta Placenta
10 chr11:71927800-71930400 Enhancers Primary hematopoietic stem cells short term culture blood
11 chr11:71928000-71929000 Weak transcription Spleen Spleen
12 chr11:71928000-71933600 Weak transcription Pancreas Pancrea
13 chr11:71928400-71930000 Enhancers Primary hematopoietic stem cells blood
14 chr11:71928400-71930000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
15 chr11:71928600-71929400 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr11:71928600-71929400 Enhancers Fetal Thymus thymus

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