chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12152603221526033AG19GENIChomozygous108694015
12152664221526643AG18GENIChomozygous108694016
12152680021526801AC17GENIChomozygous120498041
12152680121526802GT17GENIChomozygous120498042
12153010921530110GA22GENIChomozygous120498044
12153026121530262GA17GENIChomozygous108694018
12153062521530626GT17GENIChomozygous108835375
12153097521530976AG9GENIChomozygous120498045
12153122721531228AG17GENIChomozygous108694019
12153138121531382TG14GENIChomozygous108694020
12153141221531413GC11GENIChomozygous108694021
12153146121531462AG9GENIChomozygous108694022
12153152621531527AG10GENIChomozygous108835376
12153192021531921TC19GENIChomozygous108694023
12153193921531940CG17GENIChomozygous108694024
12153194321531944GA17GENIChomozygous108694025
12153217821532179TC19GENIChomozygous108694026
12153313621533137TC16GENIChomozygous108835379
12153365621533657TC18GENIChomozygous108694029
12153007221530073TC22GENIChomozygous120653297
12153007321530074GA22GENIChomozygous120653299
12153010621530107CT23GENIChomozygous120653301
12153132421531325GA17GENIChomozygous120653303
12153322521533226T23GENIChomozygous130813714
12153391421533915GA26GENIChomozygous120653305
12153417421534194AGGGGTTCCCCGACTGTAAA17GENIChomozygous130813716
12153420621534208TG19GENIChomozygous133798767
12153431521534316AG25GENIChomozygous108694031
12153435721534358AG26GENIChomozygous108694032
12153483921534840TC26GENIChomozygous108694034
12153537421535376AT12GENIChomozygous130813717
12153539521535396AG14GENIChomozygous108694035
12153640121536401TAATGTT22GENIChomozygous131981688
12153651721536518GA22GENIChomozygous109471421