chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142969659142969660TG14GENIChomozygous60877099
1142969696142969697GC20GENIChomozygous60877100
1142970867142970868GA32GENICpossibly homozygous60877101
1142971868142971869AG14GENIChomozygous60877102
1142971898142971899CT5GENIChomozygous60877103
1142973136142973137CA27GENIChomozygous60877107
1142973419142973420AG22GENICpossibly homozygous60877108
1142973904142973905CT5GENIChomozygous60877109
1142974005142974006AT21GENIChomozygous60877110
1142974097142974098AC14GENICpossibly homozygous60877111
1142974721142974722CT5GENIChomozygous60877112