chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1649761734976174CA4GENIChomozygous125646029
1650352125035213GT15GENIChomozygous125646068
1650352135035214TG14GENIChomozygous125646070
1650413485041349AT14GENIChomozygous112144517
1650413495041350AT14GENIChomozygous111704971
1651368255136826CT7GENIChomozygous125646417
1652417895241790GT6GENIChomozygous125678752
1652417965241797TC6GENIChomozygous125678753
1652630305263031AT4GENICheterozygous125678754
1652914715291472AT8GENIChomozygous111705561
1652916055291606CA6GENICheterozygous111705575
1653226065322607TA22GENIChomozygous111924141
1653616365361637TC15GENIChomozygous125646447
1654244015424402CA20GENIChomozygous125646458
1654263145426315TC10GENIChomozygous125646460
1654532745453275AT3GENICheterozygous125678755
1654593655459366CA5GENICheterozygous125678756
1654809455480946CG23GENIChomozygous111706416
1654824305482431GT17GENIChomozygous125646462
1654825575482558AT8GENIChomozygous111706434
1654825705482571AG4GENIChomozygous111706436
1654825755482576CG4GENIChomozygous111706438
1654826245482625CT6GENIChomozygous125646466
1655241915524192CT4GENIChomozygous125678757
1655493805549381TG3GENICheterozygous125678758
1655516585551659AC14GENIChomozygous125646492
1656017725601773AG3GENICheterozygous125678759
1657910515791052CA9GENIChomozygous125646516
1657911095791110CT11GENIChomozygous125646518