chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5143485148143485149CT14GENICpossibly homozygous625059372
5143489159143489160AC17GENICpossibly homozygous625059373
5143489322143489323GA20GENICpossibly homozygous625059374
5143489800143489801CT26GENICpossibly homozygous625059375
5143491429143491430AG9GENICpossibly homozygous625059376
5143492236143492237CT19GENIChomozygous625059377
5143492336143492337AT7GENIChomozygous625059378
5143492550143492551GA15GENIChomozygous625059379
5143494974143494975CT22GENICpossibly homozygous625059380
5143495081143495082AAGCAT3GENIChomozygous740696698
5143496622143496623TC25GENICpossibly homozygous625059381
5143500737143500739TA--3GENICheterozygous740696700
5143501668143501669CT18GENIChomozygous625059382
5143504816143504817CT21GENICpossibly homozygous625059383
5143504944143504945TTAA2GENICheterozygous740696702
5143505501143505502GGAAA7GENICheterozygous740696703
5143506093143506094GA13GENICheterozygous625059384
5143509248143509249A-14GENIChomozygous740696704
5143512103143512104CT18GENICpossibly homozygous625059385
5143513169143513181GTGTGTGTGTGT------------1GENIChomozygous740696705
5143519278143519279TA25GENICpossibly homozygous625059386
5143519809143519810CG16GENIChomozygous625059387
5143522265143522266TTG3GENICheterozygous740696709
5143522505143522506T-8GENIChomozygous740696710
5143526655143526656AG23GENIChomozygous625059388
5143527141143527142AC7GENICheterozygous625059389
5143527395143527396TC15GENIChomozygous625059390
5143529180143529181AT10GENIChomozygous625059391
5143529368143529369CT29GENICpossibly homozygous625059392