rs11175398 chr12:64457198 G>A

Sequence
tctgtcagtgacgatgagataagc[G/A]tacatgggggaggggctgtttcct
ASB in cell types
K562 (myelogenous leukemia) CTV-1 (Adult T acute lymphoblastic leukemia)
ASB for transcription factors
MEIS2_HUMAN PKNX1_HUMAN NCOR1_HUMAN

Color scale

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

Details

Uniprot ID
Effect size Ref
Effect size Alt
FDR Ref
FDR Alt
Mean BAD
Motif fold change
Motif concordance
MEIS2_HUMAN n/a 1.53 1.008.5·10-3 2.00 n/a No Hit
PKNX1_HUMAN n/a 1.42 1.000.03 2.00 n/a No Hit
NCOR1_HUMAN -0.94 1.71 1.000.03 2.00 n/a n/a
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Motif analysis

No data available

Genetic associations

GRASP advanced age-related macular degeneration,  aortic valve calcium,  asthma,  chronic kidney disease,  obesity with early age of onset (age >2),  recurrent major depressive disorder,  serum creatinine,  tetrology of fallot,  total cholesterol,  transmission distortion,  triglycerides
GTEx eQTL Adipose_Subcutaneous,  Adrenal_Gland,  Artery_Tibial,  Cells_Cultured_fibroblasts,  Esophagus_Mucosa,  Esophagus_Muscularis,  Heart_Atrial_Appendage,  Heart_Left_Ventricle,  Lung,  Muscle_Skeletal,  Nerve_Tibial,  Spleen,  Testis

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