chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG16GENIChomozygous952486503
5172497364172497365CT19GENIChomozygous952486504
5172499346172499347GA32GENIChomozygous952486505
5172500362172500363CT15GENIChomozygous952486506
5172501606172501607AC7GENIChomozygous952486507
5172502815172502816TG15GENIChomozygous952486508
5172502911172502912AT22GENIChomozygous952486509
5172502934172502935CT25GENIChomozygous952486510
5172505791172505792GA14GENIChomozygous952486511
5172506043172506044AG14GENIChomozygous952486512
5172506077172506078CT16GENIChomozygous952486513
5172513051172513052AG38GENIChomozygous952486514
5172514801172514802CT24GENIChomozygous952486515
5172514993172514994AG17GENIChomozygous952486516
5172515264172515265CT22GENIChomozygous952486517
5172515860172515861CT32GENIChomozygous952486518
5172516910172516911AC20GENIChomozygous952486519
5172518163172518164GA24GENIChomozygous952486520
5172518373172518374TC18GENIChomozygous952486521
5172519862172519863AC15GENIChomozygous952486522
5172525073172525074TC29GENIChomozygous952486523
5172525452172525453TC18GENIChomozygous952486524
5172526703172526704CT15GENIChomozygous952486525
5172527818172527819GT19GENIChomozygous952486526
5172528082172528083GT10GENIChomozygous952486527
5172528722172528723CT26INTERGENIChomozygous952486528
5172531253172531254AG25INTERGENICpossibly homozygous952486529
5172532496172532497TC20INTERGENIChomozygous952486530
5172538388172538389AC18INTERGENIChomozygous952486531
5172539936172539937CT23INTERGENIChomozygous952486532
5172542497172542498CG12INTERGENIChomozygous952486533