chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45214776052147761AG15GENIChomozygous112650860
45214793752147938AG25GENIChomozygous112650861
45214818552148186AT21GENIChomozygous112650862
45214819852148199TA22GENIChomozygous112650863
45215217452152175TC15GENIChomozygous119337723
45215280252152803CT30GENIChomozygous112650864
45215312352153124AC19GENIChomozygous112650865
45215480352154804CG24GENIChomozygous112650869
45215519352155194GA14GENIChomozygous112650870
45215635652156357TC18GENIChomozygous112650871
45215673852156739GA27GENIChomozygous112650872
45215750552157506GA21GENIChomozygous112650873
45215777152157772TA14GENIChomozygous112650874
45215791552157916TC23GENICpossibly homozygous112650875
45215974152159742GA27GENIChomozygous112650876
45215979152159792TC31GENIChomozygous112650877
45216033852160339CT22GENIChomozygous112650878
45216265852162659TG15GENIChomozygous112650879
45216502652165027AG27GENIChomozygous112650881
45216510152165102CT29GENIChomozygous112650882
45216511152165112GT28GENIChomozygous112650883
45216590952165910AC8GENIChomozygous112650884
45216608552166086TA17GENICheterozygous112650885
45216611652166117CA15GENICheterozygous112650886