chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4182944561182944562TC10GENIChomozygous57024895
4182944772182944773GC20GENIChomozygous57024896
4182945789182945790C-26GENIChomozygous57024897
4182946737182946738CG4GENIChomozygous57024898
4182947032182947033TC17GENIChomozygous57024899
4182947124182947125TTC16GENIChomozygous57024900
4182948641182948642TTTTTTTTG9GENICpossibly homozygous58597373
4182948659182948660GGT12GENIChomozygous57024902
4182948970182948971TC10GENIChomozygous57024903
4182948974182948983AAAAAAAAA---------7GENICheterozygous57024904
4182949798182949799CT15GENIChomozygous57024905
4182949919182949920AG25GENIChomozygous57024906
4182950045182950046CCA21GENIChomozygous57024907
4182950293182950294CT13GENIChomozygous57024908
4182952773182952774TC9GENIChomozygous57024914
4182949164182949165A-5GENICheterozygous57353923
4182950914182950915G-10GENICpossibly homozygous57024910
4182951920182951921CT12GENIChomozygous57024911
4182952502182952503GT8GENICpossibly homozygous57024912
4182952657182952658CT8GENIChomozygous57024913
4182953187182953188CA19GENIChomozygous57024915
4182953198182953199CA18GENIChomozygous57024916
4182953348182953349GA14GENIChomozygous57024917
4182953365182953366CT13GENIChomozygous57024918
4182953538182953539CT11GENIChomozygous57024919
4182954824182954825GT13GENIChomozygous57024920
4182955044182955045TA23GENIChomozygous57024921
4182955091182955092CG19GENIChomozygous57024922