chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101891145018911462ATCATCATCATC------------21GENIChomozygous52432708
101891382918913831AA--23GENICheterozygous51630222
101891383018913831A-23GENICheterozygous51630223
101891435018914351TA26GENIChomozygous51630224
101891467418914675GA29GENIChomozygous51630225
101891488318914884AG37GENIChomozygous51337789
101891494218914946GAAT----16GENIChomozygous51630226
101891514518915146AAAG31GENIChomozygous51337795
101891599818915999TC22GENIChomozygous51337802
101891634818916349CT37GENICpossibly homozygous51630227
101891704418917045GA42GENIChomozygous51630228
101891868918918690GA3GENICheterozygous51337817
101891868918918690G-3GENICheterozygous52432710
101891869118918693TG--3GENICheterozygous52432712
101891893118918932AG22GENIChomozygous51337821
101891903118919032GT19GENIChomozygous51630229
101891904218919043AG20GENIChomozygous51630230
101892025318920254GA40GENIChomozygous51630231
101892058618920587CT43GENIChomozygous51630232
101892107118921072CT15GENIChomozygous51337831
101892111318921115AC--8GENICpossibly homozygous52358488
101892157118921572TC31GENIChomozygous51337837
101892275218922753GA32INTERGENIChomozygous51630235