chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6118077154118077155GA10GENIChomozygous55264367
6118077361118077362AAC9GENICpossibly homozygous55264370
6118078311118078312T-10GENICheterozygous54960124
6118079775118079776AAT13GENIChomozygous54960128
6118080884118080900ACACACACACACACAC----------------12GENIChomozygous55532939
6118081377118081378CCGTTATTGTTTACTTCAAACATCA20GENICheterozygous56268119
6118081477118081479AG--23GENIChomozygous55264373
6118081781118081782TC32GENIChomozygous55264376
6118082601118082602GT15GENIChomozygous55264378
6118084267118084268TC17GENIChomozygous55264381
6118084598118084599CT14GENIChomozygous55264383