chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12152582821525829GC28GENIChomozygous108835366
12152603221526033AG22GENIChomozygous108694015
12152628821526289TC38GENIChomozygous108835367
12152659421526595AC11GENIChomozygous108835368
12152664221526643AG20GENICpossibly homozygous108694016
12152759721527598GA33GENIChomozygous108835369
12152764821527649GT40GENIChomozygous108835370
12152778221527783CT39GENIChomozygous108835371
12152826121528262CT24GENIChomozygous108835372
12152847321528474CA26GENIChomozygous108835373
12152853221528533TG21GENIChomozygous108835374
12152991821529919TC26GENIChomozygous108694017
12153026121530262GA15GENIChomozygous108694018
12153062521530626GT26GENIChomozygous108835375
12153122721531228AG33GENIChomozygous108694019
12153138121531382TG29GENIChomozygous108694020
12153141221531413GC27GENIChomozygous108694021
12153152621531527AG12GENIChomozygous108835376
12153192021531921TC20GENIChomozygous108694023
12153193921531940CG23GENIChomozygous108694024
12153194321531944GA22GENIChomozygous108694025
12153217821532179TC18GENIChomozygous108694026
12153285221532853GA8GENIChomozygous108835377
12153291821532919GA8GENICpossibly homozygous108835378
12153313621533137TC7GENIChomozygous108835379
12153483921534840TC29GENIChomozygous108694034
12153569021535691GT20GENICpossibly homozygous108835380
12153663021536631GA13GENIChomozygous108835381
12153676721536768CT21GENIChomozygous108835382
12153678621536787CT24GENIChomozygous108835383
12153692421536925TG25GENIChomozygous108835384
12153712521537126TC23GENIChomozygous108835385
12153712721537128TC21GENIChomozygous108835386
12153749821537499AG27GENIChomozygous108835387
12153752621537527AG21GENIChomozygous108835388
12153764121537642TC20GENIChomozygous108835389
12153279821532799TG13GENICpossibly homozygous109039988
12152877821528779GC16GENIChomozygous109039987