chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
188073927080739271AG35GENICheterozygous46670536
188074489880744899AG26GENIChomozygous46533439
188074819880748199GT20GENIChomozygous46670554
188075017180750172GA21GENIChomozygous46533441
188075045380750454TC16GENICpossibly homozygous46533443
188075103880751039GT23GENIChomozygous46533445
188075211780752118TTTTTAACC6GENIChomozygous46533449
188075266580752666GGT2GENIChomozygous46533451
188075388480753885CT32GENICpossibly homozygous46533453
188075409080754091TC23GENICpossibly homozygous46533455
188075178780751788AAG4GENIChomozygous46823701
188075178880751789AAG5GENIChomozygous46823702
188076048680760487GT15GENIChomozygous46533459
188076096380760964AT5GENICheterozygous46533461
188076130180761302AG13GENIChomozygous46533463
188076824180768242CT18GENIChomozygous46533465
188076868680768687CG25GENICpossibly homozygous46533467
188076932680769327AC10GENICpossibly homozygous46533469
188077073280770733CT25GENICheterozygous46670585