chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8125085057125085058AG16GENIChomozygous186839693
8125085221125085222TC15GENIChomozygous186839694
8125087768125087769CT17GENIChomozygous184741216
8125088350125088351GA18GENIChomozygous186839695
8125088843125088844TC19GENIChomozygous184741217
8125090107125090108GA16GENIChomozygous184741218
8125091150125091151GT20GENIChomozygous184741219
8125091360125091361CT14GENIChomozygous186839696
8125091477125091478GA21GENICpossibly homozygous184741220
8125091658125091659TC20GENIChomozygous184741221
8125091663125091664GA20GENIChomozygous184741222
8125091874125091875CA13GENIChomozygous184741223
8125093651125093652GA20GENIChomozygous184741224
8125093966125093967GC4GENIChomozygous186839697
8125095578125095579GA19GENIChomozygous184741225
8125096085125096086GT7GENICheterozygous186839698
8125096278125096279AG19GENIChomozygous184741226