Variant report

Variant rs381469
Chromosome Location chr22:22391642-22391643
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22389200-22394400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr22:22390000-22393800 Enhancers Primary B cells from cord blood blood
3 chr22:22390200-22394600 Enhancers Primary B cells from peripheral blood blood
4 chr22:22390400-22393600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
5 chr22:22390600-22391800 Enhancers Primary Natural Killer cells fromperipheralblood blood
6 chr22:22390800-22393200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr22:22390800-22393600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr22:22391000-22393200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr22:22391000-22397400 Weak transcription Right Atrium heart
10 chr22:22391200-22392000 Enhancers GM12878-XiMat blood
11 chr22:22391400-22392000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr22:22391600-22393000 Enhancers Hela-S3 cervix
13 chr22:22391600-22393600 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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