chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51467969414679695AG27GENIChomozygous137384694
51467993514679936CT22GENIChomozygous137384695
51468469014684691TC27GENIChomozygous137384696
51468503914685040TC25GENIChomozygous137384697
51468579014685791GA31GENIChomozygous137384698
51469079214690793AC14GENIChomozygous137384699
51469178414691785AG25GENIChomozygous137384700
51469440414694405CT22GENIChomozygous137384701
51469688614696887CG17GENICpossibly homozygous137384702
51469933314699334AT18GENICpossibly homozygous154264964
51469933314699334A18GENICheterozygous403891982
51470335714703358AC25GENICpossibly homozygous137384703
51470609814706099AG12GENICheterozygous154264966
51470610214706103A12GENICheterozygous403891983
51470610214706103AG12GENICheterozygous403891984
51470668914706690TA33GENIChomozygous137384704
51470753714707538TC32GENIChomozygous137384705
51470610014706101AG12GENICheterozygous403592752
51470609814706099A12GENICheterozygous403592750
51470610014706101A12GENICheterozygous403592751
51469216814692168ACAC18GENIChomozygous137291855