chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG62GENICpossibly homozygous780379466
5172491419172491420GA60GENICheterozygous780379467
5172497364172497365CT48GENIChomozygous780379468
5172499346172499347GA54GENIChomozygous780379469
5172500362172500363CT55GENIChomozygous780379470
5172501606172501607AC58GENIChomozygous780379471
5172502815172502816TG58GENIChomozygous780379472
5172502911172502912AT49GENIChomozygous780379473
5172502934172502935CT53GENIChomozygous780379474
5172505791172505792GA55GENIChomozygous780379475
5172506043172506044AG49GENIChomozygous780379476
5172506077172506078CT56GENIChomozygous780379477
5172509534172509535AG37GENIChomozygous780379478
5172513051172513052AG39GENIChomozygous780379479
5172514801172514802CT48GENIChomozygous780379480
5172514993172514994AG68GENIChomozygous780379481
5172515264172515265CT60GENIChomozygous780379482
5172515860172515861CT68GENIChomozygous780379483
5172516444172516445AT50GENICheterozygous780379484
5172516910172516911AC52GENIChomozygous780379485
5172518163172518164GA67GENICpossibly homozygous780379486
5172518373172518374TC64GENIChomozygous780379487
5172518771172518772AG19GENIChomozygous780379488
5172519862172519863AC49GENIChomozygous780379489
5172525073172525074TC65GENIChomozygous780379490
5172525452172525453TC56GENIChomozygous780379491
5172526703172526704CT52GENIChomozygous780379492
5172527818172527819GT43GENICpossibly homozygous780379493
5172528082172528083GT42GENIChomozygous780379494
5172528722172528723CT51GENICpossibly homozygous780379495
5172531253172531254AG52GENIChomozygous780379496
5172532496172532497TC50GENIChomozygous780379497
5172538388172538389AC60GENIChomozygous780379498
5172539936172539937CT45GENIChomozygous780379499
5172542497172542498CG62GENIChomozygous780379500
5172543127172543128CT36GENIChomozygous780379501