chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91474049514740496CT44GENIChomozygous142131548
91474278214742783GA55GENIChomozygous142131549
91474281714742818AC54GENIChomozygous138522502
91474314814743149CG48GENIChomozygous138522503
91474349414743495AG55GENIChomozygous142131550
91474352214743523GT53GENIChomozygous142131551
91474352514743526GA51GENIChomozygous142131552
91474687814746879TA38GENIChomozygous138522505
91475024214750243GC40GENIChomozygous138522507
91475050614750507GA46GENIChomozygous142131553
91475054714750548GA51GENIChomozygous138522508
91475678614756787GA48GENIChomozygous142131554
91476007514760076GA45GENIChomozygous142131555
91476279314762794GA36GENIChomozygous142131556
91476283214762833GT40GENIChomozygous138522511
91476573514765736GC28GENIChomozygous142131557
91476842714768428TG44GENIChomozygous142131558
91476971914769720TC42GENIChomozygous138522514
91476972814769729GA41GENIChomozygous142131559
91477112914771130TC47GENIChomozygous138522515
91477128714771288AG51GENIChomozygous138522516
91475024114750241A38GENIChomozygous138448534
91474427714744277T47GENICpossibly homozygous142109646
91475135414751354GGTAGCAGGCTAGCCCAGAGCTAGCTGTACAGAT34GENIChomozygous142109647
91476927414769278GTGG45GENIChomozygous138448535
91477433814774339TC30GENIChomozygous142131560
91477613814776139AG38GENIChomozygous138522518
91477699314776993TAAA40GENIChomozygous142109648
91477724814777249TC41GENIChomozygous138522519
91477777514777776GA31GENIChomozygous138522520
91477558314775584A19GENIChomozygous403259197
91477558314775584AG19GENICheterozygous154559778
91477558514775586AG20GENIChomozygous154559779
91477558514775586A20GENICheterozygous403259198