chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101891144418911462ATCATCATCATCATCATC------------------12GENIChomozygous51630215
101891382918913831AA--13GENICpossibly homozygous51630222
101891383018913831A-13GENICheterozygous51630223
101891435018914351TA27GENIChomozygous51630224
101891467418914675GA28GENIChomozygous51630225
101891488318914884AG25GENIChomozygous51337789
101891494218914946GAAT----21GENIChomozygous51630226
101891514518915146AAAG24GENIChomozygous51337795
101891599818915999TC15GENIChomozygous51337802
101891634818916349CT18GENIChomozygous51630227
101891704418917045GA27GENIChomozygous51630228
101891893118918932AG14GENIChomozygous51337821
101891903118919032GT19GENIChomozygous51630229
101891904218919043AG17GENIChomozygous51630230
101892025318920254GA19GENIChomozygous51630231
101892058618920587CT15GENIChomozygous51630232
101892107118921072CT12GENIChomozygous51337831
101892111318921115AC--4GENICheterozygous52358488
101892157118921572TC28GENIChomozygous51337837
101892275218922753GA37INTERGENIChomozygous51630235