rs289818 chr15:63503638 A>G

Sequence
agaggtcagagggtcagggatcca[A/G]tctccatacagatcaacaagttac
ASB in cell types
K562 (myelogenous leukemia) HCASMC (Human coronary artery smooth muscle cells)
ASB for transcription factors
CTCF_HUMAN TCF21_HUMAN

Color scale

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

Details

Uniprot ID
Effect size Ref
Effect size Alt
FDR Ref
FDR Alt
Mean BAD
Motif fold change
Motif concordance
CTCF_HUMAN 0.45 1.12 0.685.8·10-3 1.02 n/a No Hit
TCF21_HUMAN 2.07 n/a 0.021.00 2.50 n/a n/a
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Motif analysis

No data available

Genetic associations

GRASP celiac disease fasting blood glucose primary rhegmatogenous retinal detachment rheumatoid arthritis
GTEx eQTL Adipose_Subcutaneous Brain_Cerebellum Esophagus_Mucosa Heart_Left_Ventricle Whole_Blood

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