chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1222452799222452800CT53GENIChomozygous109449734
1222455486222455486AAGC39GENICpossibly homozygous134780259
1222455873222455877AAAG38GENIChomozygous134780260
1222455955222455956CT43GENIChomozygous108995507
1222455972222455973AG45GENIChomozygous109449736
1222456675222456676GA55GENIChomozygous109449737
1222456682222456683CT54GENIChomozygous109449738
1222456713222456714CT57GENIChomozygous108995508
1222457644222457645GA48GENIChomozygous109449739
1222458422222458422CAGAGCGGGATC45GENIChomozygous127486149
1222459639222459639C53GENIChomozygous127486150
1222459837222459838CT55GENIChomozygous108546733