rs11160533 chr14:99609436 C>T

Sequence
ggcaaacactgaggtccagtgaaa[C/T]aaggattgtccaggaaaccccatg
ASB in cell types
HepG2 (hepatoblastoma) glioblastoma patient-derived cell model
ASB for transcription factors
CTCF_HUMAN RBM25_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
CTCF_HUMAN 2.40 -2.18 1.9·10-41.00 1.25 n/a No Hit
RBM25_HUMAN n/a 2.70 1.000.01 4.00 n/a n/a
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Motif analysis

No data available

Genetic associations

GRASP 2 hour glucose,  abnormal involuntary movement scale,  bipolar disorder, gender differentiated,  early response to treatment in pediatric acute lymphoblastic leukemia treatment,  end-of-induction minimal residual disease (pediatric acute lymphoblastic leukemia treatment),  methotrexate clearance in pediatric acute lymphoblastic leukemia treatment
GTEx eQTL Adipose_Subcutaneous,  Adrenal_Gland,  Artery_Aorta,  Artery_Coronary,  Artery_Tibial,  Brain_Cerebellar_Hemisphere,  Colon_Sigmoid,  Colon_Transverse,  Esophagus_Gastroesophageal_Junction,  Esophagus_Mucosa,  Pituitary,  Skin_Not_Sun_Exposed_Suprapubic,  Skin_Sun_Exposed_Lower_leg,  Spleen,  Stomach,  Testis,  Thyroid

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