Variant report

Variant rs10418368
Chromosome Location chr19:19095191-19095192
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:19084200-19107800 Weak transcription Right Atrium heart
2 chr19:19091800-19096000 Weak transcription Fetal Lung lung
3 chr19:19094200-19098000 Enhancers Primary monocytes fromperipheralblood blood
4 chr19:19094400-19096000 Enhancers Primary neutrophils fromperipheralblood blood
5 chr19:19094600-19095400 Bivalent Enhancer Adipose Nuclei Adipose
6 chr19:19094800-19095600 Enhancers Spleen Spleen
7 chr19:19094800-19096400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
8 chr19:19094800-19097400 Weak transcription Right Ventricle heart
9 chr19:19094800-19097800 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr19:19094800-19099200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
11 chr19:19095000-19095200 Enhancers Brain Cingulate Gyrus brain
12 chr19:19095000-19095200 Enhancers Brain Inferior Temporal Lobe brain
13 chr19:19095000-19095600 Bivalent Enhancer Fetal Muscle Leg muscle
14 chr19:19095000-19096000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr19:19095000-19096000 Enhancers Brain Germinal Matrix brain

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