chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3161930835161930836TC14GENIChomozygous141561962
3161931278161931279GT22GENIChomozygous144654151
3161932043161932044CT18GENIChomozygous141561963
3161932281161932287TCCAGG17GENIChomozygous141486058
3161932678161932679TC19GENIChomozygous141561964
3161932865161932866GA20GENIChomozygous141561965
3161933617161933618TG19GENIChomozygous141561966
3161934401161934402GA19GENIChomozygous141561967
3161934806161934809AAG18GENIChomozygous141486059
3161934954161934955TC18GENIChomozygous141561968
3161935631161935632GA24GENIChomozygous141561969
3161935941161935941GC26GENICpossibly homozygous141486060