chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109435563594355636AG28GENIChomozygous116826350
109436047794360478CT39GENIChomozygous116685060
109436130694361307CA32GENIChomozygous116826352
109436192794361928CT25GENIChomozygous116826354
109436208694362087CT34GENIChomozygous116826356
109436219694362197AT32GENIChomozygous116685064
109436260494362605CT35GENIChomozygous116826358
109436261794362618TG37GENIChomozygous116685068
109436268694362687TC45GENIChomozygous116826360
109436335494363355CA53GENIChomozygous116826362
109436348194363482AG40GENIChomozygous116685072
109436526194365262CT32GENIChomozygous116826364
109436556194365562AC32GENIChomozygous116826366
109436571594365716TC45GENIChomozygous116826368
109436586194365862GA40GENIChomozygous116826370
109436673894366739CT27GENIChomozygous116826372
109436812594368126GA38GENIChomozygous116685082
109436838494368385GC28GENIChomozygous116685084
109436854494368545AG27GENIChomozygous116906907
109437039494370395GA20GENIChomozygous116826376
109437224194372242TC39GENIChomozygous116826378
109437233994372340CT25GENIChomozygous116826380
109437355794373558TC25GENIChomozygous116826382
109437646294376463CT24GENIChomozygous116826386
109437651794376518CT21GENIChomozygous116826388
109437751694377517CT29GENIChomozygous116826390
109437949594379496GA30GENIChomozygous116826392
109437975894379759GT36GENIChomozygous116826394
109438003094380031CT45GENIChomozygous116826396
109438030394380304TC33GENIChomozygous116826398
109438040594380406CT17GENIChomozygous116826400
109438187494381875TA41GENIChomozygous116826402
109438252794382528GT35GENIChomozygous116826404
109438416094384161TG12GENIChomozygous116906909