chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1180013908180013909AG42GENIChomozygous60981511
1180013982180013983GA42GENIChomozygous60981513
1180013990180013991TC43GENIChomozygous60981515
1180014062180014063TTGCCATCCTGAG14GENIChomozygous60981518
1180014172180014173T-20GENIChomozygous60981520
1180014224180014227CTC---21GENIChomozygous60981521
1180014301180014302AG23GENIChomozygous60981522