chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159931733159931734GA58GENIChomozygous114073602
5159931790159931791GA45GENIChomozygous114073603
5159933671159933671G15GENIChomozygous128265655
5159933675159933676AG15GENIChomozygous114652024
5159936882159936883TC69GENIChomozygous114073604
5159937645159937646TC41GENIChomozygous114073605
5159938314159938315TC41GENIChomozygous114073607
5159938574159938574TG27GENIChomozygous128265656
5159938591159938592TC30GENIChomozygous114073608
5159939921159939922CT42GENIChomozygous114073609
5159940114159940115AG59GENIChomozygous114073610
5159940390159940391CT52GENIChomozygous114073611
5159940391159940392CA53GENIChomozygous114073612
5159940410159940411AG55GENIChomozygous114073613
5159940919159940920AC51GENIChomozygous114073614
5159941486159941490ATTC10GENICheterozygous128265657
5159944166159944167AC13GENIChomozygous114073616
5159944581159944582GT51GENIChomozygous114073617
5159944742159944743GA44GENIChomozygous114073618
5159944930159944931CT54GENIChomozygous114073619
5159945573159945574AC56GENIChomozygous114073620
5159945939159945940CA59GENIChomozygous114073621
5159945943159945944TA58GENIChomozygous114073622
5159945948159945949GA56GENIChomozygous114073623
5159945949159945950CT56GENIChomozygous114073624
5159945953159945954CT54GENIChomozygous114073625
5159945991159945992CT49GENIChomozygous114073626