chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4182944561182944562TC2GENIChomozygous57024895
4182944772182944773GC11GENIChomozygous57024896
4182945789182945790C-1GENIChomozygous57024897
4182946737182946738CG4GENICheterozygous57024898
4182947032182947033TC8GENICpossibly homozygous57024899
4182947124182947125TTC15GENIChomozygous57024900
4182948659182948660GGT1GENIChomozygous57024902
4182949798182949799CT23GENICpossibly homozygous57024905
4182949919182949920AG10GENIChomozygous57024906
4182950045182950046CCA16GENIChomozygous57024907
4182950293182950294CT11GENIChomozygous57024908
4182952502182952503GT12GENIChomozygous57024912
4182951920182951921CT5GENIChomozygous57024911
4182952657182952658CT17GENIChomozygous57024913
4182952773182952774TC3GENIChomozygous57024914
4182953187182953188CA2GENIChomozygous57024915
4182953198182953199CA8GENIChomozygous57024916
4182953348182953349GA11GENICpossibly homozygous57024917
4182953365182953366CT14GENIChomozygous57024918
4182953538182953539CT20GENIChomozygous57024919
4182954824182954825GT6GENIChomozygous57024920
4182955044182955045TA11GENICpossibly homozygous57024921
4182955091182955092CG10GENIChomozygous57024922