chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101891144418911462ATCATCATCATCATCATC------------------15GENIChomozygous51630215
101891382918913831AA--15GENICpossibly homozygous51630222
101891383018913831A-15GENICheterozygous51630223
101891435018914351TA30GENIChomozygous51630224
101891467418914675GA30GENIChomozygous51630225
101891488318914884AG22GENIChomozygous51337789
101891494218914946GAAT----12GENIChomozygous51630226
101891514518915146AAAG33GENIChomozygous51337795
101891599818915999TC28GENIChomozygous51337802
101891634818916349CT21GENIChomozygous51630227
101891704418917045GA30GENIChomozygous51630228
101891893118918932AG24GENIChomozygous51337821
101891903118919032GT29GENIChomozygous51630229
101891904218919043AG31GENIChomozygous51630230
101892025318920254GA32GENIChomozygous51630231
101892058618920587CT23GENIChomozygous51630232
101892107118921072CT20GENIChomozygous51337831
101892157118921572TC33GENIChomozygous51337837
101892275218922753GA36INTERGENIChomozygous51630235
101891382818913829CCCAAAAAAAA15GENICheterozygous52358486
101892111318921115AC--11GENICheterozygous52358488
101891865818918659AAAATAATAAT2GENIChomozygous52482441