chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149944263149944264TTGG2GENIChomozygous57952462
4149944781149944782AAC6GENIChomozygous56979626
4149944947149944948CT6GENIChomozygous57952465
4149945888149945889GA5GENICheterozygous57952468
4149950205149950206CG12GENIChomozygous57952471
4149957525149957526AG11GENIChomozygous57952473
4149958382149958383CT8GENIChomozygous57952476
4149958776149958777GC15GENIChomozygous57952479
4149961986149961987AT8GENICpossibly homozygous57952482
4149964471149964472CA13GENIChomozygous56979642
4149967945149967946AG14GENIChomozygous56979647
4149968400149968401TTCC2GENICheterozygous57839761
4149968400149968401TTC2GENICheterozygous58777275
4149968683149968684CT10GENICpossibly homozygous56979649
4149976078149976079CT15GENIChomozygous57952485
4149982801149982802AT1GENIChomozygous56979680
4149983026149983028AG--4GENIChomozygous56979681
4149983665149983666GA15GENIChomozygous56979682
4149983739149983740CT20GENICpossibly homozygous57839762
4149984063149984064GA5GENIChomozygous56979683
4149984103149984104GA10GENIChomozygous57839764
4149984708149984709TC11GENIChomozygous56979684
4149984808149984809AC14GENICpossibly homozygous56979685
4149984840149984841AG8GENIChomozygous56979686
4149985089149985090CT2GENIChomozygous56979687
4149985325149985326AC17GENICpossibly homozygous56979688
4149985437149985438CT13GENICheterozygous56979689
4149985527149985528AG8GENIChomozygous56979690
4149986007149986008AG10GENIChomozygous56979692