chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
725509852550986TC64GENIChomozygous780638492
725529902552991CT57GENIChomozygous780638493
725548192554820TC53GENIChomozygous780638494
725548782554879AG64GENIChomozygous780638495
725607292560730TA44GENIChomozygous780638496
725632342563235GC63GENICheterozygous780638497
725632342563235GT63GENICheterozygous780638498
725672442567245GA76GENICpossibly homozygous780638499
725682602568261AT49GENIChomozygous780638500
725697932569794CT47GENIChomozygous780638501
725706912570692TC30GENICpossibly homozygous780638502
725719322571933AG70GENICpossibly homozygous780638503
725729912572992TA51GENIChomozygous780638504
725732352573236TC72GENIChomozygous780638505
725738912573892GA54GENIChomozygous780638506
725747452574746AT57GENICheterozygous780638507
725747652574766AT65GENICheterozygous780638508
725748672574868TA229GENICheterozygous780638509
725749292574930AT227GENICheterozygous780638510
725749612574962AT197GENICheterozygous780638511
725780582578059CT2GENIChomozygous780638512
725787172578718AC10GENIChomozygous780638513
725787192578720AG10GENIChomozygous780638514
725787292578730GC15GENIChomozygous780638515
725788792578880AC38GENIChomozygous780638516
725790132579014CT35GENICpossibly homozygous780638517
725819322581933CT52GENIChomozygous780638518
725829822582983TC41GENIChomozygous780638519
725864832586484CT38GENICpossibly homozygous780638520
725867762586777TC73GENICpossibly homozygous780638521
725908852590886AT32GENIChomozygous780638522
725914992591500CT47GENICpossibly homozygous780638523