chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157836030157836031AT28GENIChomozygous112907444
4157836227157836228GA29GENIChomozygous112907446
4157836572157836573CT21GENIChomozygous112907448
4157837504157837505GA21GENIChomozygous112907450
4157837831157837832CG34GENIChomozygous112907452
4157837839157837840CT33GENIChomozygous112907454
4157841215157841216TC28GENIChomozygous112907466
4157841427157841428AC31GENIChomozygous112907468
4157841700157841701AG25GENIChomozygous112907470
4157842052157842053CT23GENIChomozygous112907472
4157842609157842610AG27GENIChomozygous112907474
4157843453157843454CT35GENIChomozygous112907476
4157843576157843577TC40GENIChomozygous112907478
4157844423157844424TC28GENIChomozygous112907480
4157844460157844461CT34GENIChomozygous112907482
4157844829157844830AG13GENIChomozygous112907484
4157844893157844894TC12GENIChomozygous112907486
4157845266157845267TC18GENIChomozygous112907488
4157845741157845742GA20GENIChomozygous112907490
4157846052157846053GA28GENIChomozygous112907492
4157846668157846669TC17GENIChomozygous112907494
4157847567157847568GA27GENIChomozygous112907506
4157847804157847805GA30GENIChomozygous112907508
4157848313157848314CT36GENIChomozygous112907510
4157850478157850479CT28GENIChomozygous112907512
4157853940157853941TG17GENIChomozygous112907518
4157854310157854311AG27GENIChomozygous112907520