chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211249147211249148CA39GENIChomozygous978014431
1211249164211249165AG35GENIChomozygous978014432
1211249514211249515AG17GENIChomozygous978014433
1211249867211249868GA29GENIChomozygous978014434
1211249879211249880GT31GENIChomozygous978014435
1211250193211250194AC51GENIChomozygous978014436
1211250496211250497TC33GENIChomozygous978014437
1211250622211250623CG43GENIChomozygous978014438
1211250623211250624CT41GENIChomozygous978014439
1211250700211250701GA40GENIChomozygous978014440
1211252203211252204AG35GENIChomozygous978014441
1211252276211252277CT16GENIChomozygous978014442
1211252677211252678CT37GENIChomozygous978014443
1211254276211254277AC35GENIChomozygous978014444
1211254477211254478TC42GENIChomozygous978014445
1211254496211254497CT42GENIChomozygous978014446
1211255440211255441GT22GENIChomozygous978014447
1211255616211255617AT40GENIChomozygous978014448
1211256722211256723TC34GENIChomozygous978014449
1211257074211257075AG27GENIChomozygous978014450
1211258234211258235GA21GENIChomozygous978014451
1211258541211258542CT43GENIChomozygous978014452
1211258803211258804TC22GENIChomozygous978014453
1211259421211259422AG15GENIChomozygous978014454
1211259737211259738AG35GENICpossibly homozygous978014455
1211259868211259869CT55GENIChomozygous978014456
1211260475211260476CG48GENIChomozygous978014457
1211261011211261012GA32GENIChomozygous978014458
1211261278211261279AG37GENIChomozygous978014459
1211261430211261431CT16GENIChomozygous978014460
1211261727211261728CT15GENIChomozygous978014461
1211262513211262514GA67GENIChomozygous978014462
1211262865211262866AG52GENIChomozygous978014463
1211263517211263518CA29GENIChomozygous978014464
1211264098211264099TG32GENIChomozygous978014465
1211264888211264889CA36GENIChomozygous978014466
1211264889211264890TA35GENIChomozygous978014467