chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159931733159931734GA14GENIChomozygous114073602
5159931790159931791GA15GENIChomozygous114073603
5159936882159936883TC22GENIChomozygous114073604
5159937645159937646TC19GENIChomozygous114073605
5159938314159938315TC16GENIChomozygous114073607
5159938591159938592TC28GENIChomozygous114073608
5159939921159939922CT23GENIChomozygous114073609
5159940114159940115AG22GENIChomozygous114073610
5159940390159940391CT28GENICpossibly homozygous114073611
5159940391159940392CA27GENICpossibly homozygous114073612
5159940410159940411AG23GENICpossibly homozygous114073613
5159940919159940920AC19GENIChomozygous114073614
5159944581159944582GT16GENIChomozygous114073617
5159944742159944743GA15GENIChomozygous114073618
5159945573159945574AC22GENIChomozygous114073620
5159945939159945940CA32GENIChomozygous114073621
5159945943159945944TA30GENIChomozygous114073622
5159945948159945949GA23GENIChomozygous114073623
5159945949159945950CT24GENIChomozygous114073624
5159945953159945954CT23GENIChomozygous114073625
5159945991159945992CT24GENIChomozygous114073626