chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149944263149944264TTGG6GENIChomozygous57952462
4149944781149944782AAC20GENIChomozygous56979626
4149944947149944948CT35GENIChomozygous57952465
4149945888149945889GA26GENIChomozygous57952468
4149950205149950206CG34GENIChomozygous57952471
4149955087149955093CAAAAA------10GENICheterozygous58473151
4149955889149955890CCGTGTGTGT2GENIChomozygous58473162
4149957185149957191ACACAC------2GENIChomozygous58473175
4149957525149957526AG31GENIChomozygous57952473
4149958382149958383CT22GENIChomozygous57952476
4149958776149958777GC24GENIChomozygous57952479
4149961986149961987AT27GENIChomozygous57952482
4149964471149964472CA39GENIChomozygous56979642
4149967945149967946AG36GENIChomozygous56979647
4149968683149968684CT30GENIChomozygous56979649
4149973218149973219CCT5GENICheterozygous56979660
4149976078149976079CT27GENIChomozygous57952485
4149982503149982504CCCCCTAGAACGAT29GENIChomozygous56979679
4149982801149982802AT26GENIChomozygous56979680
4149983026149983028AG--12GENIChomozygous56979681
4149983665149983666GA26GENIChomozygous56979682
4149984063149984064GA29GENIChomozygous56979683
4149984708149984709TC28GENIChomozygous56979684
4149984808149984809AC27GENIChomozygous56979685
4149984840149984841AG27GENIChomozygous56979686
4149985089149985090CT23GENIChomozygous56979687
4149985325149985326AC26GENIChomozygous56979688
4149985437149985438CT37GENIChomozygous56979689
4149985527149985528AG23GENIChomozygous56979690
4149985905149985906C-7GENIChomozygous56979691
4149986007149986008AG18GENIChomozygous56979692
4149973218149973219CCTTT5GENICheterozygous57348956
4149967399149967400T-23GENICpossibly homozygous58345958
4149968400149968401TTCC6GENIChomozygous57839761
4149983739149983740CT21GENIChomozygous57839762
4149984103149984104GA24GENIChomozygous57839764