chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1461751986175199TG10GENIChomozygous874949510
1461767686176769AT22GENIChomozygous874949511
1461771496177150TC28GENIChomozygous874949512
1461774006177401GC18GENIChomozygous874949513
1461774566177457TC23GENIChomozygous874949514
1461775596177560AG17GENIChomozygous874949515
1461776266177627AG14GENIChomozygous874949516
1461778266177827AG11GENIChomozygous874949517
1461811396181140GA10GENIChomozygous874949327
1462160386216039TC17GENIChomozygous874949518
1462166006216601CT7GENIChomozygous874949519
1462189296218930CT21GENIChomozygous874949520
1462189636218964CG17GENIChomozygous874949521
1462193116219312CT14GENIChomozygous874949522
1462194456219446GA17GENIChomozygous874949523
1462196006219601GA22GENIChomozygous874949524
1462202146220215CG9GENIChomozygous874949525
1462202236220224CT12GENIChomozygous874949526
1462204066220407GA5GENIChomozygous874949527
1462205506220551TA6GENIChomozygous874949528
1462207146220715AG12GENIChomozygous874949529
1462207476220748TC10GENIChomozygous874949530
1462208026220803AG7GENIChomozygous874949531
1462208036220804CT7GENIChomozygous874949532
1462209816220982AG17GENIChomozygous874949533
1462212306221231TC6GENIChomozygous874949534
1462229226222923CT4GENIChomozygous874949535
1462235806223581TC20GENICheterozygous874949536
1462236656223666CG28GENIChomozygous874949537
1462238206223821AG18GENICpossibly homozygous874949538
1462248436224844AG20GENIChomozygous874949539
1462250206225021TC23GENIChomozygous874949540
1462251516225152CA6GENIChomozygous874949541
1462253816225382TC15GENIChomozygous874949542
1462255256225526GA7GENIChomozygous874949543
1462256946225695AG13GENIChomozygous874949544
1462261626226163GA17GENIChomozygous874949545
1462267716226772CT10GENIChomozygous874949546