chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG31GENIChomozygous114092623
5172497364172497365CT31GENIChomozygous114092625
5172499346172499347GA47GENIChomozygous114092627
5172500362172500363CT41GENIChomozygous114092629
5172501606172501607AC26GENIChomozygous114092631
5172502815172502816TG19GENIChomozygous114092633
5172502911172502912AT25GENICpossibly homozygous114092635
5172502934172502935CT27GENIChomozygous114092637
5172505791172505792GA38GENIChomozygous114092639
5172506077172506078CT47GENIChomozygous114092643
5172514801172514802CT37GENICpossibly homozygous114092649
5172514993172514994AG38GENIChomozygous114092651
5172515264172515265CT35GENIChomozygous114092653
5172515860172515861CT31GENIChomozygous114092655
5172516910172516911AC27GENIChomozygous114092659
5172518163172518164GA32GENICpossibly homozygous114092661
5172518373172518374TC40GENIChomozygous114092663
5172519862172519863AC17GENIChomozygous114092667
5172525073172525074TC28GENIChomozygous114092669
5172525452172525453TC20GENIChomozygous114092671
5172526703172526704CT16GENIChomozygous114092673
5172527818172527819GT26GENIChomozygous114092675
5172528082172528083GT16GENIChomozygous114092677
5172528722172528723CT29GENIChomozygous114092679
5172531253172531254AG19GENIChomozygous114092681
5172532496172532497TC28GENIChomozygous114092683
5172538388172538389AC31GENIChomozygous114092685
5172539936172539937CT28GENIChomozygous114092687
5172542099172542100AG11GENICheterozygous119064738
5172542100172542101CT11GENICheterozygous119064739
5172542497172542498CG18GENIChomozygous114092689
5172543127172543128CT13GENIChomozygous114092691