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rs5027681 chr5:116365059 C>T

Sequence
ccaatgtcatcactcagaaaatga[C/T]agtgagaaagacatggtttgtcca
ASB in cell types
K562 (myelogenous leukemia)
ASB for transcription factors
MEIS2_HUMAN PBX2_HUMAN PKNX1_HUMAN

Color scale

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

Details

Uniprot ID
Effect size Ref
Effect size Alt
FDR Ref
FDR Alt
Mean BAD
Motif fold change
Motif concordance
MEIS2_HUMAN 2.95 n/a 2.9·10-101.00 2.00 n/a No Hit
PBX2_HUMAN 2.43 n/a 4.8·10-31.00 2.00 n/a No Hit
PKNX1_HUMAN 2.04 n/a 0.021.00 1.67 n/a No Hit
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Motif analysis

No data available

Genetic associations

GRASP paternal transmission distortion
GTEx eQTL Adipose_Subcutaneous Adipose_Visceral_Omentum Brain_Amygdala Brain_Caudate_basal_ganglia Brain_Cerebellar_Hemisphere Brain_Cerebellum Brain_Hippocampus Brain_Hypothalamus Brain_Spinal_cord_cervical_c-1 Breast_Mammary_Tissue Cells_Cultured_fibroblasts Esophagus_Muscularis Heart_Atrial_Appendage Liver Lung Muscle_Skeletal Nerve_Tibial Skin_Sun_Exposed_Lower_leg Testis Thyroid

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