chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG43GENIChomozygous794079576
5172497364172497365CT43GENIChomozygous794079577
5172499346172499347GA37GENIChomozygous794079578
5172500362172500363CT32GENIChomozygous794079579
5172501606172501607AC39GENICpossibly homozygous794079580
5172502815172502816TG27GENICpossibly homozygous794079581
5172502911172502912AT38GENIChomozygous794079582
5172502934172502935CT44GENIChomozygous794079583
5172505791172505792GA41GENIChomozygous794079584
5172506043172506044AG34GENIChomozygous794079585
5172506077172506078CT37GENIChomozygous794079586
5172509534172509535AG26GENIChomozygous794079587
5172513051172513052AG31GENIChomozygous794079588
5172514801172514802CT28GENIChomozygous794079589
5172514993172514994AG35GENIChomozygous794079590
5172515264172515265CT43GENIChomozygous794079591
5172515860172515861CT50GENIChomozygous794079592
5172516444172516445AT27GENICheterozygous794079593
5172516910172516911AC38GENIChomozygous794079594
5172518163172518164GA40GENIChomozygous794079595
5172518373172518374TC37GENIChomozygous794079596
5172518771172518772AG10GENIChomozygous794079597
5172519862172519863AC43GENIChomozygous794079598
5172525073172525074TC48GENIChomozygous794079599
5172525452172525453TC36GENIChomozygous794079600
5172526703172526704CT35GENICpossibly homozygous794079601
5172527818172527819GT29GENIChomozygous794079602
5172528082172528083GT28GENICpossibly homozygous794079603
5172528722172528723CT38GENIChomozygous794079604
5172531253172531254AG34GENIChomozygous794079605
5172532496172532497TC52GENIChomozygous794079606
5172538388172538389AC41GENIChomozygous794079607
5172539936172539937CT39GENIChomozygous794079608
5172542497172542498CG28GENIChomozygous794079609
5172543127172543128CT25GENIChomozygous794079610