chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34552658045526581AG18GENIChomozygous111554427
34552663545526636GA19GENIChomozygous111554428
34552699645526997CT17GENIChomozygous111554429
34552739945527400CT6GENIChomozygous112272082
34552757845527579CT24GENIChomozygous111554430
34552774445527745AG24GENIChomozygous111554431
34552811645528117TC25GENIChomozygous111554432
34552830245528303TA21GENIChomozygous111554433
34552928645529287AG22GENIChomozygous111554435
34552932745529328GA20GENIChomozygous111554436
34552937445529375AT22GENIChomozygous111554437
34552953745529538AG12GENIChomozygous111554438
34552978945529790GC17GENIChomozygous111554439
34553388245533883TC22GENIChomozygous111554443
34553400145534002TA25GENIChomozygous111554444
34553503645535037AC25GENIChomozygous111554445
34553524745535248TC28GENIChomozygous111554446
34553638145536382GC19GENIChomozygous111554448
34553692045536921AC10GENIChomozygous111554449
34553918345539184CA21GENIChomozygous112272086
34553989245539893GA21GENIChomozygous112272087
34554184645541847GA21GENIChomozygous111554465
34554285645542857TC19GENIChomozygous111554473
34554356445543565AG23GENIChomozygous111554477
34554465245544653AG21GENIChomozygous112272094
34554623045546231CT25GENICpossibly homozygous112272095
34554666345546664GA13GENIChomozygous112272096
34554719845547199CT28GENIChomozygous111554490
34554722845547229GA26GENIChomozygous111554491
34554996045549961CT21GENIChomozygous112272098
34554996245549963CG20GENIChomozygous112272099
34555000645550007GA21GENIChomozygous112272100
34555021945550220TA14GENIChomozygous112272101
34555105945551060AG16GENIChomozygous111554498
34555222545552226GA23GENIChomozygous112272104