chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31674159816741599CT51GENICpossibly homozygous57173447
31674221616742217GA49GENIChomozygous57173449
31674296016742961A-4GENIChomozygous57173451
31674586316745864CCT27GENIChomozygous57173453
31674622916746230CG45GENICheterozygous57173455
31674708316747084TG64GENIChomozygous57173457
31674716716747168AG51GENIChomozygous57173459
31674768216747717CAGGTCCTGGCTTACGGTAAGGAAAGCCGTACCAC-----------------------------------8GENIChomozygous57173461
31674957916749580GA48GENICpossibly homozygous57173463
31674968916749690CT53GENIChomozygous57173465
31674969916749700TC49GENIChomozygous57173467
31674980616749807CT47GENIChomozygous57173469
31675003016750031AG47GENIChomozygous57173471
31675025116750252AG39GENICpossibly homozygous57173473
31675050816750509TC38GENIChomozygous57173475
31675057616750577CCTTTT5GENIChomozygous57173477
31675098016750981CT34GENIChomozygous57173479
31675143616751437GA30GENICheterozygous57173481
31675144016751441TTA25GENICheterozygous57173483
31675144216751443GGC27GENIChomozygous57173485
31675168416751685GA43GENIChomozygous57173487
31675179716751798TA37GENICheterozygous57173489
31675179916751800TTTTC28GENICpossibly homozygous57173491
31675437616754377GA41GENIChomozygous57173499
31675235216752353GC41GENIChomozygous57173493
31675280516752806GA44GENICpossibly homozygous57173495
31675389916753900TG51GENIChomozygous57173497
31675505616755057AG37GENIChomozygous57173501
31675539816755399TG54GENIChomozygous57173503
31675557416755575GA33GENICheterozygous57173505
31675561316755614TC36GENICheterozygous57173507
31675562216755623AG31GENIChomozygous57173508
31675680016756801TTAGGG44GENIChomozygous57173510
31675775016757751GA67GENIChomozygous57173512