chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159915649159915650TC6GENIChomozygous114073573
5159915836159915837AG9GENIChomozygous114073574
5159916035159916036AG6GENIChomozygous114073575
5159916154159916155GA4GENIChomozygous114073576
5159916314159916315GA7GENIChomozygous114073577
5159916621159916622CT14GENIChomozygous114073578
5159916663159916664CT11GENIChomozygous114073579
5159917376159917377TC6GENIChomozygous114073580
5159917595159917596TC8GENIChomozygous114073581
5159917634159917635AG8GENIChomozygous114073582
5159918095159918096AG10GENIChomozygous114073583
5159918567159918568AC10GENIChomozygous114073584
5159919346159919347GA7GENIChomozygous114073585
5159919424159919425AG9GENIChomozygous114073586
5159928048159928049CT6GENICheterozygous114073590
5159928312159928313CT13GENIChomozygous114073591
5159928446159928447GA7GENIChomozygous114073592
5159928593159928594CT9GENIChomozygous114073594
5159929653159929654AC4GENIChomozygous114073595
5159930049159930050CT5GENIChomozygous114073596
5159930265159930266CT5GENIChomozygous114073597
5159930774159930775TA4GENIChomozygous114073601