chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18005349480053495GA11GENIChomozygous142834800
18005415980054160TA14GENIChomozygous142834801
18005436580054366GC10GENIChomozygous142834802
18005457780054578AG9GENIChomozygous142834803
18005483680054837AG11GENIChomozygous142834804
18005569480055695GA10GENIChomozygous142834805
18005632080056321TC21GENIChomozygous142834806
18005697180056993CACACACACACACACACACACG14GENIChomozygous142788640
18005706780057068GA20GENIChomozygous142834807
18005708580057085A23GENIChomozygous142788641
18005708680057086A22GENIChomozygous142788642
18005716480057165GA23GENIChomozygous142834808
18005778180057782CT23GENIChomozygous142834809
18005834680058347GT15GENIChomozygous142834810
18005837480058375AG13GENIChomozygous142834811
18005858380058584C5GENIChomozygous403699396
18005858880058589TC5GENICheterozygous403699399
18005815480058155A5GENICheterozygous403699394
18005815480058155AT5GENICheterozygous403699395
18005858380058584CA5GENICheterozygous403699397
18005858880058589T5GENIChomozygous403699398
18005908080059081TC6GENICheterozygous147244420
18005908080059081T6GENICheterozygous403699400
18005974680059747CT17GENIChomozygous142834812
18005988380059884TC19GENIChomozygous142834813
18006034180060342AC15GENIChomozygous142834814
18006145980061460AG11GENIChomozygous142834815
18006172580061725GTCTGTGTC18GENIChomozygous142788643
18006185080061851GA16GENIChomozygous142834816
18006220780062208CT10GENIChomozygous142834817
18006223680062236GCTCTACCACTGAGCCACGCCCCCAGCCCCTCACTGGGGGATTCTAGGCAGGGAGGA6GENIChomozygous142788644
18006308780063088GA17GENIChomozygous143785361
18006613080066131TA19GENICpossibly homozygous142834818
18006679180066791T8GENIChomozygous142788645
18006714880067149CT12GENIChomozygous142834819