chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71489250614892507TG17GENIChomozygous115575939
71489298614892987AC20GENIChomozygous115575940
71489316614893167GA15GENIChomozygous115575941
71489347214893472CCT14GENIChomozygous128437229
71489405914894060AT13GENIChomozygous115575942
71489596314895963CTCCTCCTTTTCTTCCTCCTCCTCCTCTTCCTCCTCCTCCTTCTCTTCCTC5GENIChomozygous132106226
71489852814898529TC23GENIChomozygous115575946
71489853614898537TC25GENIChomozygous115575947
71489929714899298AC20GENIChomozygous115575948
71490226514902266GA21GENIChomozygous115575949
71490328114903282C23GENIChomozygous128437230
71490358014903580AACA21GENIChomozygous128437231
71490398314903984TC15GENIChomozygous115575950
71490440414904404TATAGA15GENIChomozygous128437232
71490480214904803G10GENIChomozygous128437233
71490487314904874GA11GENIChomozygous115575951
71490651814906519GA20GENIChomozygous115575952
71490657314906574GA21GENICpossibly homozygous115575953
71490664014906641AT22GENIChomozygous115575954
71490670814906709CT17GENIChomozygous115575955
71490671114906712TC18GENIChomozygous115575956
71490681014906811CT19GENIChomozygous115575957
71490682514906826AG21GENIChomozygous115575958
71490683414906835CG20GENIChomozygous115575959