Variant_ID,RSID,Chromosome,Position,Reference_Allele,Alternate_Allele,Joint_AF,Non_Finnish_European_AF,Evo2_7B_AvgRC_Delta,Evo2_40B_AvgRC_Delta,Functional_Annotation,Gene,Exonic_Function,Amino_Acid_Change,ENCODE_cCRE_Annotation,PhastCons_100way,PhyloP_100way
19:44908684:T:C,rs429358,19,44908684,T,C,0.14852,0.15063,9.21533012390137,15.9466071128845,exonic,APOE,nonsynonymous SNV,APOE:ENST00000252486.9:exon4:c.T388C:p.C130R,Coding,0.904,2.086