chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18892305288923053AG27GENIChomozygous108884571
18892371488923715AG9GENIChomozygous108884573
18892547388925474AG22GENIChomozygous108884574
18892559188925592CT26GENIChomozygous120503094
18892572488925725CT26GENIChomozygous120503095
18892714088927141TG35GENIChomozygous120503096
18892806988928070TG34GENIChomozygous109307626
18892814988928150CT24GENIChomozygous108884578
18892893188928932AC28GENICpossibly homozygous120668692
18892979888929799TA17GENIChomozygous120503098
18892980188929802TA16GENIChomozygous120503099
18893039788930398TA20GENIChomozygous108884583
18893076488930765GA23GENIChomozygous108884585
18893535788935358GC20GENIChomozygous108884588
18893618688936187CT20GENIChomozygous120668694
18893658388936584GC21GENIChomozygous109307673
18893668188936682AG19GENIChomozygous120503100
18893773888937739CT28GENIChomozygous108884589
18893982688939827CT20GENIChomozygous109307677
18894076488940765GC17GENIChomozygous108884591
18894101288941013AG6GENIChomozygous109307679
18894195488941955CT20GENIChomozygous109307688
18894237888942379GT38GENIChomozygous120668696
18894284088942841CA39GENIChomozygous109307690
18894293588942936GA33GENIChomozygous120668698
18894393888943939AG15GENIChomozygous108884593
18894599288945993GA19GENIChomozygous108884595
18894616388946164TC19GENIChomozygous108884596
18894705588947056GC20GENIChomozygous109307694
18894848788948488TC20GENIChomozygous108884599
18894957988949580CT22GENIChomozygous109307696