chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101891144418911462ATCATCATCATCATCATC------------------17GENIChomozygous51630215
101891382818913829CCCAAAAAAAA12GENICheterozygous52358486
101891382918913831AA--12GENICheterozygous51630222
101891383018913831A-12GENICheterozygous51630223
101891435018914351TA25GENIChomozygous51630224
101891467418914675GA24GENIChomozygous51630225
101891488318914884AG25GENIChomozygous51337789
101891494218914946GAAT----18GENIChomozygous51630226
101891514518915146AAAG33GENIChomozygous51337795
101891599818915999TC14GENIChomozygous51337802
101891634818916349CT34GENIChomozygous51630227
101891704418917045GA28GENIChomozygous51630228
101891865818918659AAAATAATAAT3GENIChomozygous52482441
101891893118918932AG15GENIChomozygous51337821
101891903118919032GT27GENIChomozygous51630229
101891904218919043AG25GENIChomozygous51630230
101892025318920254GA28GENIChomozygous51630231
101892058618920587CT31GENIChomozygous51630232
101892107118921072CT20GENIChomozygous51337831
101892111318921115AC--4GENICheterozygous52358488
101892157118921572TC25GENIChomozygous51337837
101892275218922753GA21INTERGENIChomozygous51630235