chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34552658045526581AG25GENIChomozygous111554427
34552663545526636GA25GENIChomozygous111554428
34552699645526997CT19GENIChomozygous111554429
34552739945527400CT15GENIChomozygous112272082
34552757845527579CT36GENIChomozygous111554430
34552774445527745AG36GENIChomozygous111554431
34552811645528117TC31GENIChomozygous111554432
34552830245528303TA31GENIChomozygous111554433
34552928645529287AG33GENIChomozygous111554435
34552932745529328GA33GENIChomozygous111554436
34552937445529375AT22GENIChomozygous111554437
34552953745529538AG25GENIChomozygous111554438
34552978945529790GC24GENIChomozygous111554439
34553388245533883TC44GENIChomozygous111554443
34553400145534002TA33GENICpossibly homozygous111554444
34553503645535037AC34GENIChomozygous111554445
34553524745535248TC39GENIChomozygous111554446
34553638145536382GC43GENIChomozygous111554448
34553692045536921AC12GENIChomozygous111554449
34553918345539184CA33GENIChomozygous112272086
34553989245539893GA26GENIChomozygous112272087
34554184645541847GA30GENIChomozygous111554465
34554285645542857TC30GENIChomozygous111554473
34554356445543565AG29GENIChomozygous111554477
34554465245544653AG36GENIChomozygous112272094
34554623045546231CT20GENIChomozygous112272095
34554666345546664GA21GENIChomozygous112272096
34554719845547199CT28GENIChomozygous111554490
34554722845547229GA30GENIChomozygous111554491
34554996045549961CT27GENIChomozygous112272098
34554996245549963CG27GENIChomozygous112272099
34555000645550007GA18GENIChomozygous112272100
34555105945551060AG40GENIChomozygous111554498