chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18005349480053495GA48GENICpossibly homozygous142834800
18005415980054160TA32GENIChomozygous142834801
18005436580054366GC29GENIChomozygous142834802
18005457780054578AG26GENIChomozygous142834803
18005483680054837AG29GENIChomozygous142834804
18005569480055695GA16GENIChomozygous142834805
18005632080056321TC37GENIChomozygous142834806
18005697180056993CACACACACACACACACACACG33GENIChomozygous142788640
18005706780057068GA28GENIChomozygous142834807
18005708580057085A29GENIChomozygous142788641
18005708680057086A30GENIChomozygous142788642
18005716480057165GA32GENIChomozygous142834808
18005778180057782CT44GENIChomozygous142834809
18005817980058179A18GENICheterozygous141162205
18005834680058347GT17GENIChomozygous142834810
18005837480058375AG13GENIChomozygous142834811
18005853580058543ACACCACA5GENIChomozygous143739856
18005908080059081TC17GENICheterozygous147244420
18005974680059747CT38GENIChomozygous142834812
18005988380059884TC33GENIChomozygous142834813
18006034180060342AC32GENIChomozygous142834814
18006145980061460AG37GENIChomozygous142834815
18006172580061725GTCTGTGTC32GENIChomozygous142788643
18006185080061851GA41GENIChomozygous142834816
18006220780062208CT35GENIChomozygous142834817
18006223680062236GCTCTACCACTGAGCCACGCCCCCAGCCCCTCACTGGGGGATTCTAGGCAGGGAGGA18GENIChomozygous142788644
18006308780063088GA35GENIChomozygous143785361
18006346480063464GG20GENIChomozygous143739857
18006613080066131TA36GENIChomozygous142834818
18006679180066791T20GENIChomozygous142788645
18006714880067149CT27GENIChomozygous142834819