chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4180469795180469796AC5GENIChomozygous126030969
4180470718180470719AG4GENICheterozygous119283861
4180470720180470721GA3GENICheterozygous119283863
4180470736180470737AG6GENIChomozygous112974637
4180479578180479579TG5GENICheterozygous126056246
4180507862180507863CA14GENICheterozygous126041479
4180528616180528617CG5GENICheterozygous126083847
4180532090180532091TC11GENIChomozygous126107071
4180578347180578348GT14GENIChomozygous126030982
4180589446180589447TC14GENIChomozygous126030984
4180617344180617345GA6GENIChomozygous126030985
4180617391180617392AT14GENIChomozygous126030986
4180636283180636284AT4GENICheterozygous112975056
4180639313180639314TC17GENICheterozygous126030988
4180640053180640054CG27GENIChomozygous126030989
4180640522180640523GT9GENIChomozygous112975081
4180640605180640606GT8GENICheterozygous112975082
4180640651180640652GA9GENIChomozygous126041481
4180640695180640696CT14GENIChomozygous126030990
4180640772180640773CT5GENIChomozygous126041482
4180646375180646376TC10GENIChomozygous126030995
4180646391180646392CT6GENIChomozygous126030996
4180646395180646396TG4GENIChomozygous126030997
4180655447180655448GT6GENICheterozygous126107072
4180660226180660227AC4GENIChomozygous126030998
4180662258180662259CA7GENIChomozygous126030999
4180668895180668896AC4GENIChomozygous112975183
4180704446180704447CG5GENICheterozygous126031004
4180707875180707876TA6GENICheterozygous126056253
4180707958180707959TC4GENICheterozygous126107073
4180735699180735700CG6GENICheterozygous126107074
4180735732180735733CG8GENICheterozygous126107075
4180775947180775948AG5GENICheterozygous126107076
4180786402180786403TC10GENIChomozygous126031009
4180786438180786439TC13GENIChomozygous126031010
4180786442180786443TC12GENIChomozygous112975696
4180786455180786456CA14GENIChomozygous126031011