chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13629622936296230CA22GENIChomozygous108075907
13629783336297834CT15GENIChomozygous109475590
13629837136298372AG41GENIChomozygous109475591
13629932236299323GA42GENIChomozygous108075926
13629934036299341CT51GENICpossibly homozygous109475592
13629960636299607TC32GENIChomozygous109475593
13629960836299609GC32GENIChomozygous109475594
13630005236300053CA32GENIChomozygous109475595
13630151436301515TC26GENIChomozygous108075935
13630161136301612AG40GENIChomozygous108075937
13630168436301685TC39GENIChomozygous109475596
13630656236306563GA34GENIChomozygous109475597
13630678736306788CT29GENIChomozygous109475598
13630860436308605TC10GENIChomozygous108075978
13630866636308667GC15GENIChomozygous108075979
13630871936308720AT23GENIChomozygous108075980
13630966636309667AG29GENIChomozygous108075989
13631410136314102GC27GENIChomozygous109475599