chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101891144418911462ATCATCATCATCATCATC------------------20GENIChomozygous51630215
101891382918913831AA--13GENICpossibly homozygous51630222
101891435018914351TA24GENIChomozygous51630224
101891467418914675GA19GENIChomozygous51630225
101891488318914884AG27GENIChomozygous51337789
101891494218914946GAAT----16GENIChomozygous51630226
101891514518915146AAAG21GENIChomozygous51337795
101891599818915999TC23GENIChomozygous51337802
101891634818916349CT31GENIChomozygous51630227
101891704418917045GA21GENIChomozygous51630228
101891382818913829CCCAAAAAAAA13GENICheterozygous52358486
101891868918918690GA4GENIChomozygous51337817
101891893118918932AG15GENIChomozygous51337821
101891903118919032GT17GENIChomozygous51630229
101891904218919043AG17GENIChomozygous51630230
101892025318920254GA30GENICpossibly homozygous51630231
101892058618920587CT34GENIChomozygous51630232
101892107118921072CT13GENIChomozygous51337831
101892111318921115AC--4GENIChomozygous52358488
101892157118921572TC20GENIChomozygous51337837
101892275218922753GA41INTERGENIChomozygous51630235