chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75846351258463516TCTC----11GENICheterozygous54420586
75846351458463516TC--11GENICheterozygous53930141
75846468658464687A-8GENICheterozygous54905138
75847325558473256T-41GENICheterozygous55081926
75847359258473616TCTCTCTCTCTCTCTCTCTGTGTG------------------------27GENICheterozygous55081928
75847355458473556GC--22GENICheterozygous55810468
75847716758477168CCGT7GENICheterozygous54977338
75847716758477168CCGTGT7GENICheterozygous54977340
75848871158488712CCA5GENICheterozygous54977342
75850632558506326GGT6GENICheterozygous54420611
75851438458514386CA--3GENICheterozygous54977344
75851454058514542CA--20GENICheterozygous55058504
75851726858517269C-7GENICheterozygous55058505
75851952058519522TC--6GENICheterozygous54977346
75852866358528664CT18GENIChomozygous53930161
75852918158529183AC--14GENICheterozygous54977350
75852923058529231TA30GENIChomozygous53930164
75854390058543901GC10GENIChomozygous54977354
75854390158543902GA10GENIChomozygous54977356
75854390358543904GC10GENIChomozygous53930168
75855640758556409AA--1GENIChomozygous54905162
75855641058556411AAGTG1GENIChomozygous55141816
75856242558562426TTAC10GENIChomozygous53930175
75856251758562521ACAC----6GENICheterozygous54420638
75856334158563342AAT3GENICheterozygous55058506
75857059458570595AAT18GENIChomozygous53930179
75857093358570934G-23GENIChomozygous53930181
75858849258588493T-15GENIChomozygous53930185
75858853858588539TTA14GENIChomozygous53930187
75858873958588740G-21GENIChomozygous53930189
75858888458588885AATG13GENICpossibly homozygous53930190
75858893458588935G-9GENICheterozygous54855535
75859556658595567CCACACACACACACACACACACACACACACACA3GENIChomozygous54977360