chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157836030157836031AT5GENIChomozygous112907444
4157836227157836228GA11GENIChomozygous112907446
4157836572157836573CT6GENICheterozygous112907448
4157837504157837505GA11GENIChomozygous112907450
4157839648157839649CA8GENIChomozygous112907458
4157840713157840714CT5GENIChomozygous112907464
4157841427157841428AC13GENIChomozygous112907468
4157841700157841701AG9GENIChomozygous112907470
4157842052157842053CT18GENICheterozygous112907472
4157842609157842610AG14GENIChomozygous112907474
4157843453157843454CT18GENIChomozygous112907476
4157843576157843577TC11GENIChomozygous112907478
4157844423157844424TC4GENIChomozygous112907480
4157844460157844461CT15GENIChomozygous112907482
4157844829157844830AG7GENIChomozygous112907484
4157845266157845267TC14GENIChomozygous112907488
4157845741157845742GA19GENIChomozygous112907490
4157846052157846053GA17GENIChomozygous112907492
4157846830157846831CG3GENICheterozygous112907504
4157847567157847568GA13GENIChomozygous112907506
4157848313157848314CT16GENIChomozygous112907510
4157850478157850479CT15GENIChomozygous112907512
4157851298157851299TC20GENICheterozygous112907514
4157851404157851405CT5GENIChomozygous112907516
4157853940157853941TG12GENIChomozygous112907518
4157854310157854311AG14GENIChomozygous112907520
4157854969157854970AG10GENICheterozygous126027733