chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159932269159932270AT11GENIChomozygous114358660
5159933309159933326TGTGTGTATGTGTGATA11GENIChomozygous130964146
5159933675159933676AG18GENIChomozygous114652024
5159933671159933671G18GENIChomozygous128265655
5159934252159934253CT19GENIChomozygous114160444
5159935564159935565TG16GENIChomozygous114160445
5159936882159936883TC27GENIChomozygous114073604
5159937100159937101AG20GENIChomozygous114160446
5159937107159937107GA23GENIChomozygous130964147
5159937645159937646TC27GENIChomozygous114073605
5159938097159938098CA8GENIChomozygous114160447
5159938314159938315TC27GENIChomozygous114073607
5159938574159938574TG22GENIChomozygous128265656
5159938591159938592TC22GENIChomozygous114073608
5159939161159939162GA23GENIChomozygous114160451
5159939327159939328CT20GENIChomozygous114358664
5159939921159939922CT27GENIChomozygous114073609
5159945948159945949GA30GENIChomozygous114073623
5159940114159940115AG20GENIChomozygous114073610
5159940919159940920AC22GENIChomozygous114073614
5159945939159945940CA32GENIChomozygous114073621
5159945943159945944TA31GENIChomozygous114073622
5159934495159934497GG4GENIChomozygous135313999
5159934499159934499GG4GENIChomozygous135314000
5159945949159945950CT30GENIChomozygous114073624
5159945953159945954CT29GENIChomozygous114073625
5159945991159945992CT28GENIChomozygous114073626
5159946459159946460GA31GENIChomozygous114358670