chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159931733159931734GA26GENIChomozygous114073602
5159931790159931791GA20GENIChomozygous114073603
5159933671159933671G14GENIChomozygous128265655
5159933675159933676AG14GENIChomozygous114652024
5159936882159936883TC14GENIChomozygous114073604
5159937645159937646TC21GENIChomozygous114073605
5159938314159938315TC17GENIChomozygous114073607
5159938574159938574TG14GENIChomozygous128265656
5159938591159938592TC16GENIChomozygous114073608
5159939921159939922CT18GENIChomozygous114073609
5159940114159940115AG26GENIChomozygous114073610
5159940390159940391CT15GENIChomozygous114073611
5159940391159940392CA15GENIChomozygous114073612
5159940410159940411AG14GENIChomozygous114073613
5159940919159940920AC17GENICpossibly homozygous114073614
5159941486159941490ATTC5GENICheterozygous128265657
5159944166159944167AC6GENIChomozygous114073616
5159944581159944582GT22GENIChomozygous114073617
5159944742159944743GA20GENIChomozygous114073618
5159944930159944931CT25GENIChomozygous114073619
5159945573159945574AC33GENIChomozygous114073620
5159945939159945940CA25GENIChomozygous114073621
5159945943159945944TA24GENIChomozygous114073622
5159945948159945949GA24GENIChomozygous114073623
5159945949159945950CT24GENIChomozygous114073624
5159945953159945954CT25GENIChomozygous114073625
5159945991159945992CT25GENIChomozygous114073626