chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4183022663183022664GGA29GENIChomozygous57025063
4183025517183025523GAGAGA------17GENIChomozygous57025069
4183025504183025505GA24GENICpossibly homozygous57559525
4183025566183025567TC23GENICheterozygous57559527
4183024349183024350TC31GENIChomozygous57559521
4183024366183024367GA30GENIChomozygous57559523
4183026660183026661CT26GENIChomozygous57559529
4183027418183027420AA--18GENIChomozygous57559531
4183028012183028013TC26GENICpossibly homozygous57559533
4183028022183028023GA26GENIChomozygous57559535
4183029418183029419GA35GENIChomozygous57559537
4183030153183030154GGTGA24GENIChomozygous57025076
4183030392183030393CT20GENIChomozygous57559539
4183030662183030663CT30GENIChomozygous57559541
4183030673183030674AG28GENIChomozygous57559543
4183030737183030738TC29GENICheterozygous57559545
4183030847183030848TC33GENICheterozygous57559547
4183032232183032233AC25GENICpossibly homozygous57559549
4183032311183032312GT21GENIChomozygous57559551
4183032618183032619AG19GENIChomozygous57025093
4183033099183033102AAA---1GENIChomozygous57559553
4183033554183033555CT14GENIChomozygous57025096
4183033622183033623AT13GENICheterozygous57025097
4183034298183034300CA--8GENIChomozygous57025098
4183035208183035211AAA---4GENIChomozygous57559555
4183035663183035664TC32GENICheterozygous57559557
4183036184183036185TC25GENIChomozygous57025104
4183036319183036333GTGTGTGTGTGTGT--------------9GENIChomozygous57025105
4183036708183036709TC14GENIChomozygous57559559
4183037103183037104GT24GENIChomozygous57025108
4183037269183037270GA21GENIChomozygous57559561
4183037794183037795TC20GENIChomozygous57025110
4183037949183037950TG17GENIChomozygous57025111
4183038145183038146GA23GENIChomozygous57559563
4183039836183039837TA30GENIChomozygous57025120
4183040348183040349CT17GENIChomozygous57559565