chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG26GENIChomozygous895989318
5172495129172495130TC18GENIChomozygous895989319
5172497364172497365CT23GENIChomozygous895989320
5172500362172500363CT21GENIChomozygous895989321
5172501621172501622TC4GENIChomozygous895989322
5172501653172501654TC18GENIChomozygous895989323
5172502815172502816TG14GENIChomozygous895989324
5172502911172502912AT22GENIChomozygous895989325
5172502934172502935CT27GENIChomozygous895989326
5172505791172505792GA22GENIChomozygous895989327
5172506043172506044AG11GENIChomozygous895989328
5172506077172506078CT14GENIChomozygous895989329
5172513051172513052AG22GENIChomozygous895989330
5172514801172514802CT12GENIChomozygous895989331
5172514993172514994AG30GENIChomozygous895989332
5172515264172515265CT17GENIChomozygous895989333
5172515860172515861CT11GENIChomozygous895989334
5172516444172516445AT4GENICheterozygous895989335
5172516910172516911AC22GENIChomozygous895989336
5172518163172518164GA11GENIChomozygous895989337
5172518373172518374TC30GENIChomozygous895989338
5172519862172519863AC8GENIChomozygous895989339
5172521173172521174TG29GENIChomozygous895989340
5172525073172525074TC10GENIChomozygous895989341
5172525452172525453TC14GENIChomozygous895989342
5172526703172526704CT16GENIChomozygous895989343
5172527818172527819GT18GENIChomozygous895989344
5172528082172528083GT15GENIChomozygous895989345
5172528722172528723CT18GENIChomozygous895989346
5172531253172531254AG14GENIChomozygous895989347
5172532496172532497TC13GENIChomozygous895989348
5172538388172538389AC21GENIChomozygous895989349
5172539936172539937CT4GENIChomozygous895989350
5172542497172542498CG15GENIChomozygous895989351
5172543127172543128CT19GENIChomozygous895989352