chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1526784922678493AC37GENICheterozygous48222365
1526804122680413CCTTCGCCGGA16GENIChomozygous48222368
1526804322680433CCT9GENIChomozygous48222370
1526804392680440C-12GENIChomozygous48222371
1526804462680447AAT6GENIChomozygous48222372
1526804502680451GGT6GENIChomozygous48222373
1526805322680533AG12GENICpossibly homozygous48222374
1526805922680597CTGAG-----14GENICheterozygous48222375
1526806372680638CG28GENIChomozygous48222376
1526808122680813G-49GENIChomozygous48222378
1526808142680815AAG51GENIChomozygous48222379
1526944762694478TC--30GENIChomozygous48222403
1527014932701494TG47GENICheterozygous48869688