chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159931733159931734GA26GENIChomozygous114073602
5159931790159931791GA20GENIChomozygous114073603
5159933671159933671G22GENIChomozygous128265655
5159933675159933676AG22GENIChomozygous114652024
5159936882159936883TC35GENIChomozygous114073604
5159937645159937646TC33GENIChomozygous114073605
5159938314159938315TC35GENIChomozygous114073607
5159938574159938574TG22GENIChomozygous128265656
5159938591159938592TC29GENIChomozygous114073608
5159939921159939922CT30GENIChomozygous114073609
5159940114159940115AG36GENIChomozygous114073610
5159940390159940391CT41GENIChomozygous114073611
5159940391159940392CA42GENIChomozygous114073612
5159940410159940411AG40GENIChomozygous114073613
5159940919159940920AC39GENIChomozygous114073614
5159941486159941490ATTC4GENICheterozygous128265657
5159944166159944167AC13GENIChomozygous114073616
5159944581159944582GT31GENIChomozygous114073617
5159945943159945944TA38GENIChomozygous114073622
5159944742159944743GA35GENIChomozygous114073618
5159944930159944931CT54GENIChomozygous114073619
5159945573159945574AC39GENIChomozygous114073620
5159945939159945940CA39GENIChomozygous114073621
5159945948159945949GA37GENIChomozygous114073623
5159945949159945950CT37GENIChomozygous114073624
5159945953159945954CT36GENIChomozygous114073625
5159945991159945992CT38GENIChomozygous114073626