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rs618145 chr9:76704644 A>C

Sequence
caggacttagtgaggcatgccttg[A/C]aaatgtagttagttttctctctac
ASB for transcription factors
CTCF_HUMAN

Color scale

color scale ref
-log10 FDR of Ref (A) ASB
color scale alt
-log10 FDR of Alt (C) ASB

Details

Uniprot ID
Effect size Ref
Effect size Alt
FDR Ref
FDR Alt
Mean BAD
Motif fold change
Motif concordance
CTCF_HUMAN 0.36 0.64 1.004.1·10-3 1.29 n/a No Hit
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Motif analysis

No data available

Genetic associations

GRASP coronary artery disease (cad), gender differentiated neuroticism
GTEx eQTL Adipose_Visceral_Omentum Brain_Cerebellar_Hemisphere Brain_Cerebellum Cells_EBV-transformed_lymphocytes Heart_Left_Ventricle Liver Lung Spleen Whole_Blood

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