chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31674159816741599CT10GENIChomozygous57173447
31674221616742217GA13GENIChomozygous57173449
31674296016742961A-14GENIChomozygous57173451
31674708316747084TG19GENIChomozygous57173457
31674716716747168AG12GENIChomozygous57173459
31674957916749580GA5GENIChomozygous57173463
31674968916749690CT9GENIChomozygous57173465
31674969916749700TC12GENIChomozygous57173467
31674980616749807CT16GENIChomozygous57173469
31675003016750031AG8GENIChomozygous57173471
31675025116750252AG3GENIChomozygous57173473
31675050816750509TC24GENIChomozygous57173475
31675057616750577CCTTTT2GENICheterozygous57173477
31675168416751685GA19GENIChomozygous57173487
31675179716751798TA12GENIChomozygous57173489
31675179916751800TTTTC14GENICpossibly homozygous57173491
31675235216752353GC9GENIChomozygous57173493
31675280516752806GA18GENIChomozygous57173495
31675389916753900TG10GENIChomozygous57173497
31675437616754377GA9GENIChomozygous57173499
31675505616755057AG11GENIChomozygous57173501
31675539816755399TG11GENIChomozygous57173503
31675562216755623AG6GENIChomozygous57173508
31675680016756801TTAGGG9GENIChomozygous57173510
31675775016757751GA24GENIChomozygous57173512
31674547216745473CA32GENIChomozygous57871630
31675641416756415CA12GENIChomozygous57871634
31674586516745866T-23GENIChomozygous58571894
31675557316755574GGATGTGTGT9GENIChomozygous58540529