chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG26GENIChomozygous114092623
5172495129172495130TC18GENIChomozygous126207709
5172497364172497365CT23GENIChomozygous114092625
5172500362172500363CT21GENIChomozygous114092629
5172501621172501622TC4GENIChomozygous126207710
5172501653172501654TC18GENIChomozygous126207711
5172502815172502816TG14GENIChomozygous114092633
5172502911172502912AT22GENIChomozygous114092635
5172502934172502935CT27GENIChomozygous114092637
5172505791172505792GA22GENIChomozygous114092639
5172506043172506044AG11GENIChomozygous114092641
5172506077172506078CT14GENIChomozygous114092643
5172513051172513052AG22GENIChomozygous114092647
5172514801172514802CT12GENIChomozygous114092649
5172514993172514994AG30GENIChomozygous114092651
5172515264172515265CT17GENIChomozygous114092653
5172515860172515861CT11GENIChomozygous114092655
5172516444172516445AT4GENICheterozygous114092657
5172516910172516911AC22GENIChomozygous114092659
5172518163172518164GA11GENIChomozygous114092661
5172518373172518374TC30GENIChomozygous114092663
5172519862172519863AC8GENIChomozygous114092667
5172521173172521174TG29GENIChomozygous126207712
5172525073172525074TC10GENIChomozygous114092669
5172525452172525453TC14GENIChomozygous114092671
5172526703172526704CT16GENIChomozygous114092673
5172527818172527819GT18GENIChomozygous114092675
5172528082172528083GT15GENIChomozygous114092677
5172528722172528723CT18GENIChomozygous114092679
5172531253172531254AG14GENIChomozygous114092681
5172532496172532497TC13GENIChomozygous114092683
5172538388172538389AC21GENIChomozygous114092685
5172539936172539937CT4GENIChomozygous114092687
5172542497172542498CG15GENIChomozygous114092689
5172543127172543128CT19GENIChomozygous114092691