chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139096852690968527AC27GENIChomozygous114575482
139096924090969241TC17GENIChomozygous114575484
139096988390969884AG23GENIChomozygous114575486
139097005690970057GT15GENIChomozygous114575488
139097009690970097GT24GENIChomozygous114575490
139097044690970447GA29GENIChomozygous114575492
139097102190971022CT31GENIChomozygous114575494
139097134590971346CT38GENIChomozygous114575496
139097147290971473AT28GENIChomozygous114575498
139097158790971588AG29GENIChomozygous114575500
139097180290971803AG14GENIChomozygous114649422
139097180590971806AG13GENIChomozygous114649424
139097214890972149AG31GENIChomozygous114575504
139097235390972354TA16GENIChomozygous114649426
139097237590972376TG21GENIChomozygous114575506
139097237790972378AT21GENIChomozygous114575508
139097411590974116TC19GENIChomozygous114575510
139097412390974124AG21GENIChomozygous114575512
139097414090974141GC29GENIChomozygous114575514
139097544290975443CT17GENIChomozygous114649428
139097548490975485AC19GENIChomozygous114649430
139097644790976448CT16GENIChomozygous114575516
139097813390978134CG24GENIChomozygous114575518
139097824290978243AG27GENIChomozygous114575520
139097848490978485AG37GENIChomozygous114575522
139097858390978584GA18GENIChomozygous114575524