chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101891145018911462ATCATCATCATC------------6GENIChomozygous52432708
101891382918913831AA--8GENICheterozygous51630222
101891383018913831A-8GENICpossibly homozygous51630223
101891456618914567GGT11GENICheterozygous51337788
101891488318914884AG19GENIChomozygous51337789
101891514518915146AAAG11GENIChomozygous51337795
101891599818915999TC20GENIChomozygous51337802
101891634818916349CT33GENIChomozygous51630227
101891435018914351TA24GENIChomozygous51630224
101891467418914675GA20GENIChomozygous51630225
101891494218914946GAAT----10GENIChomozygous51630226
101891704418917045GA19GENIChomozygous51630228
101891868918918690G-1GENIChomozygous52432710
101891869118918693TG--1GENIChomozygous52432712
101891893118918932AG13GENIChomozygous51337821
101891903118919032GT12GENIChomozygous51630229
101891904218919043AG13GENIChomozygous51630230
101892025318920254GA21GENIChomozygous51630231
101892058618920587CT30GENIChomozygous51630232
101892107118921072CT12GENIChomozygous51337831
101892111318921115AC--3GENIChomozygous52358488
101892157118921572TC14GENIChomozygous51337837
101892275218922753GA18INTERGENIChomozygous51630235