chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37755217277552173AC14GENIChomozygous598963506
37755282577552826AG33GENIChomozygous598963507
37755286477552865CG25GENIChomozygous598963508
37755310477553105AG27GENIChomozygous598963509
37755347877553479CT28GENIChomozygous604877844
37755391777553918G-34GENIChomozygous728620623
37755467277554673CT22GENIChomozygous598963510
37755717277557173GA31GENIChomozygous598963511
37755796177557962A-14GENIChomozygous728620624
37756013477560135GA34GENIChomozygous598963512
37756058777560588AT5GENIChomozygous598963513
37756105977561060GA25GENIChomozygous604877845
37756156277561563TA35GENIChomozygous604877846
37756163877561639CA25GENIChomozygous598963514
37756240977562410TG30GENIChomozygous604877847
37756310277563103TTA27GENICpossibly homozygous728620625
37756310377563104TA28GENICpossibly homozygous598963515
37756390077563901GA37GENIChomozygous604877848
37756444977564450GA23GENIChomozygous598963516
37756471577564716T-16GENIChomozygous728620626
37756494877564950TT--18GENIChomozygous728620627
37756499077564991GA16GENIChomozygous598963517
37756514177565142AAT17GENICheterozygous728620631
37756514277565143T-17GENICheterozygous728620630
37756569877565699GGA18GENIChomozygous728620632
37756570577565706GGTGT16GENIChomozygous728620634
37756730477567305C-31GENIChomozygous728620635
37756772577567726GT30GENIChomozygous598963518
37756855977568560AAAGGGTTACTGGAAT30GENIChomozygous728620636
37756867777568680GGG---16GENIChomozygous728620637
37756883477568835AG32GENICpossibly homozygous598963519
37756965177569654TTG---34GENIChomozygous728620639