chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12152582821525829GC15GENIChomozygous108835366
12152603221526033AG18GENIChomozygous108694015
12152628821526289TC17GENIChomozygous108835367
12152659421526595AC15GENIChomozygous108835368
12152664221526643AG13GENIChomozygous108694016
12152759721527598GA12GENIChomozygous108835369
12152764821527649GT19GENIChomozygous108835370
12152778221527783CT21GENIChomozygous108835371
12152826121528262CT16GENIChomozygous108835372
12152847321528474CA11GENIChomozygous108835373
12152853221528533TG17GENIChomozygous108835374
12152991821529919TC19GENIChomozygous108694017
12153026121530262GA16GENIChomozygous108694018
12153062521530626GT14GENIChomozygous108835375
12153122721531228AG20GENIChomozygous108694019
12153138121531382TG13GENIChomozygous108694020
12153141221531413GC10GENIChomozygous108694021
12153192021531921TC15GENIChomozygous108694023
12153193921531940CG8GENIChomozygous108694024
12153194321531944GA10GENIChomozygous108694025
12153217821532179TC12GENIChomozygous108694026
12153285221532853GA14GENIChomozygous108835377
12153291821532919GA9GENICheterozygous108835378
12153313621533137TC5GENIChomozygous108835379
12153483921534840TC14GENIChomozygous108694034
12153569021535691GT11GENIChomozygous108835380
12153663021536631GA13GENIChomozygous108835381
12153676721536768CT16GENIChomozygous108835382
12153678621536787CT13GENIChomozygous108835383
12153692421536925TG16GENICheterozygous108835384
12153712521537126TC7GENIChomozygous108835385
12153712721537128TC6GENIChomozygous108835386
12153749821537499AG21GENIChomozygous108835387
12153752621537527AG19GENIChomozygous108835388
12153764121537642TC19GENIChomozygous108835389
12153635521536356GA5GENICheterozygous125474926