chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
52957390229573903TC19GENIChomozygous775217599
52957396529573966GA39GENIChomozygous775217600
52957405529574056AG43GENIChomozygous775217601
52957410829574109TC48GENIChomozygous775217602
52957425929574260GA41GENIChomozygous775217603
52957427529574276GT31GENIChomozygous775217604
52957469929574700GA32GENIChomozygous775217605
52957492929574930GA37GENIChomozygous775217606
52957493429574935CG35GENIChomozygous775217607
52957498329574984AG30GENIChomozygous775217608
52957520929575210GA49GENIChomozygous775217609
52957591129575912TC54GENIChomozygous775217610
52957686929576870CT57GENICpossibly homozygous775217611
52957746929577470TC26GENIChomozygous775217612
52957757129577572TG41GENICpossibly homozygous775217613
52957757229577573TC40GENIChomozygous775217614
52957781129577812GC35GENIChomozygous775217615
52957787729577878GA49GENIChomozygous775217616
52957827129578272TC55GENIChomozygous775217617
52957925329579254CT63GENIChomozygous775217618
52957994729579948CT37GENIChomozygous775217619
52958011629580117GA73GENIChomozygous775217620
52958176129581762CT21GENIChomozygous775217621
52958243829582439AG51GENIChomozygous775217622
52958416029584161GA61GENICpossibly homozygous775217623
52958596529585966CT42GENIChomozygous775217624
52958672029586721CT38GENIChomozygous775217625
52958769329587694GA30GENICpossibly homozygous775217626
52959226729592268GA23GENIChomozygous775217627
52959312429593125AG28GENIChomozygous775217628
52959415629594157TC27GENIChomozygous775217629
52959867629598677AG45GENIChomozygous775217630
52960064929600650TC32GENIChomozygous775217631
52960099529600996AG28GENIChomozygous775217632