chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4496094244960943TA15GENIChomozygous108706687
X4496291244962913CT11GENIChomozygous108706689
X4496728044967281TC16GENIChomozygous108489575
X4496780744967808TC7GENIChomozygous108489577
X4496942244969423TC15GENIChomozygous108489579
X4497169144971692AC12GENIChomozygous108706691
X4497386444973864T7GENIChomozygous132778919
X4497482044974821CT18GENIChomozygous108489585
X4497584644975846T13GENIChomozygous132778920
X4497747844977479A9GENIChomozygous132778921
X4497768544977686CA7GENIChomozygous108706693
X4497936344979364AG15GENIChomozygous108489591
X4497973944979740CT16GENIChomozygous108489593
X4498179644981797AC15GENIChomozygous108489597
X4498217844982179AG7GENIChomozygous108706695
X4498341644983417AT13GENIChomozygous108706697
X4498639444986395CA10GENIChomozygous108489601
X4498085244980989GACTCTTTCCATCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCGC5GENICheterozygous133518733
X4498144344981444T7GENIChomozygous133454207
X4498265244982652AGAGACAGAG5GENIChomozygous133454208
X4498844244988442A6GENIChomozygous132248218