chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206650348206650349AG52GENIChomozygous61067523
1206650370206650371AAAC42GENICpossibly homozygous61067524
1206650803206650804GA44GENIChomozygous61067525
1206651096206651097GA45GENIChomozygous61067526
1206653027206653035TGTGTGTC--------9GENICheterozygous62314594
1206654412206654413AC38GENIChomozygous61067527
1206658200206658212TATCTATGTATC------------1GENIChomozygous62192988
1206658280206658281CCATCT6GENIChomozygous61067528
1206661128206661129GA52GENIChomozygous61067529
1206661774206661775A-27GENIChomozygous61067530
1206662661206662662TTCA2GENICheterozygous61067531
1206664470206664480CTCCCTCTCT----------9GENICheterozygous62192990
1206664574206664576AC--20GENIChomozygous61067532
1206664613206664614CCACATAT22GENIChomozygous61067533
1206664639206664647TATATATA--------24GENICheterozygous62302122
1206664641206664647TATATA------24GENICheterozygous62192992
1206664710206664711AG36GENIChomozygous61067537
1206665220206665223TAC---17GENIChomozygous61067538
1206666699206666700GA31GENIChomozygous61067539
1206668089206668090GA32GENIChomozygous61067540
1206668764206668776GTGTGTGTATGT------------5GENICheterozygous62192994