rs13195812 chr6:167030414 C>T

Sequence
aatcagatttccacttctccttct[C/T]ggccctgacagtgcctggtttctg
ASB in cell types
K562 (myelogenous leukemia)
ASB for transcription factors
ARI1B_HUMAN IKZF1_HUMAN NR2C1_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
ARI1B_HUMAN 2.83 -2.82 4.1·10-31.00 1.00 n/a n/a
IKZF1_HUMAN 2.42 -2.26 0.021.00 1.00 n/a n/a
NR2C1_HUMAN 2.07 -0.13 0.040.84 1.00 n/a No Hit
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Motif analysis

No data available

Genetic associations

GRASP graves disease,  ldl cholesterol,  triglycerides
GTEx eQTL Adipose_Subcutaneous,  Adipose_Visceral_Omentum,  Brain_Cerebellar_Hemisphere,  Brain_Cerebellum,  Cells_Cultured_fibroblasts,  Esophagus_Mucosa,  Esophagus_Muscularis,  Heart_Atrial_Appendage,  Heart_Left_Ventricle,  Lung,  Nerve_Tibial,  Pancreas,  Prostate,  Skin_Not_Sun_Exposed_Suprapubic,  Skin_Sun_Exposed_Lower_leg,  Thyroid,  Whole_Blood

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