chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131415136131415137TC23GENIChomozygous137622926
5131415442131415443GA23GENIChomozygous143960626
5131415458131415458G23GENIChomozygous137342141
5131415460131415462CA22GENIChomozygous137342142
5131416339131416340TG18GENIChomozygous137622929
5131417992131417993TC17GENIChomozygous143960627
5131418041131418042GC21GENICpossibly homozygous137622931
5131418692131418693GA21GENIChomozygous143960628
5131418808131418809AG6GENIChomozygous137622933
5131418826131418827A11GENICheterozygous403158134
5131418824131418825AT11GENIChomozygous154337120
5131418824131418825A11GENICheterozygous403158133
5131418826131418827AT11GENIChomozygous154337121
5131418828131418829A11GENICheterozygous403158135
5131418828131418829AT11GENICheterozygous403158136
5131418830131418831A11GENICheterozygous403158137
5131418830131418831AT11GENICheterozygous403158138
5131418870131418871TA17GENIChomozygous154337126
5131418870131418871T17GENICheterozygous403158139
5131419456131419457TA27GENIChomozygous137622934
5131421064131421065CT26GENIChomozygous143960629
5131421490131421491AT19GENIChomozygous143960630
5131422478131422479AT8GENIChomozygous143960631
5131422550131422551AC4GENIChomozygous143960632