chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1229163353229163354C-19GENICpossibly homozygous61108398
1229163505229163506GA64GENIChomozygous61108399
1229164413229164415CT--27GENICpossibly homozygous61108400
1229164413229164416CTT---27GENICheterozygous61108401
1229164414229164416TT--22GENICpossibly homozygous61108402
1229165744229165745CT42GENIChomozygous61108403
1229165924229165925A-48GENIChomozygous61108404
1229166503229166504GA51GENIChomozygous61108405
1229167530229167532GG--5GENICheterozygous61108406
1229167543229167545GT--18GENICheterozygous61108407
1229169570229169571CA15GENIChomozygous61108408