chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159932440159932441AT21GENIChomozygous798665447
5159934252159934253CT24GENIChomozygous798665448
5159934477159934478GT11GENICheterozygous798665449
5159935564159935565TG41GENIChomozygous798665450
5159936882159936883TC40GENIChomozygous798665451
5159937100159937101AG23GENIChomozygous798665452
5159937645159937646TC31GENIChomozygous798665453
5159938097159938098CA55GENICheterozygous798665454
5159938134159938135TA38GENICheterozygous798665455
5159938314159938315TC26GENIChomozygous798665456
5159938591159938592TC37GENIChomozygous798665457
5159938719159938720CT39GENICpossibly homozygous798665458
5159939093159939094GA37GENIChomozygous798665459
5159939161159939162GA32GENIChomozygous798665460
5159939364159939365GA25GENIChomozygous798665461
5159940055159940056GA37GENIChomozygous798665462
5159940114159940115AG30GENIChomozygous798665463
5159940919159940920AC41GENIChomozygous798665464
5159941201159941202GT36GENIChomozygous798665465
5159944581159944582GT28GENIChomozygous798665466
5159944691159944692GT38GENIChomozygous798665467
5159944742159944743GA46GENIChomozygous798665468
5159944930159944931CT32GENIChomozygous798665469
5159945573159945574AC43GENIChomozygous798665470
5159945939159945940CA34GENIChomozygous798665471
5159945943159945944TA33GENIChomozygous798665472
5159945948159945949GA33GENIChomozygous798665473
5159945949159945950CT33GENIChomozygous798665474
5159945953159945954CT35GENIChomozygous798665475
5159945991159945992CT51GENIChomozygous798665476