chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155294274155294275CT33GENIChomozygous929178595
5155294360155294361TC14GENIChomozygous929178596
5155295748155295749TC36GENIChomozygous929178597
5155300981155300982TG62GENIChomozygous929178598
5155302190155302191GA45GENIChomozygous929178599
5155307760155307761AG45GENIChomozygous929178600
5155308085155308086CT49GENIChomozygous929178601
5155308199155308200AC63GENIChomozygous929178602
5155308271155308272CT51GENIChomozygous929178603
5155308396155308397TC37GENIChomozygous929178604
5155308975155308976TC29GENIChomozygous929178605
5155309320155309321TG48GENIChomozygous929178606
5155309638155309639TG36GENIChomozygous929178607
5155309712155309713CT33GENIChomozygous929178608
5155311340155311341TC44GENIChomozygous929178609
5155311536155311537GC38GENIChomozygous929178610
5155311877155311878AG47GENIChomozygous929178611
5155311999155312000AG24GENIChomozygous929178612
5155312352155312353AT46GENIChomozygous929178613
5155316409155316410AG47GENIChomozygous929178614
5155316472155316473TA46GENIChomozygous929178615
5155316661155316662CT48GENIChomozygous929178616
5155316675155316676TG46GENIChomozygous929178617
5155317165155317166TC34GENIChomozygous929178618
5155318171155318172CT48GENIChomozygous929178619
5155318392155318393CT28GENIChomozygous929178620
5155318688155318689AG43GENIChomozygous929178621
5155319466155319467GA32GENIChomozygous929178622