chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221645792221645793TC20GENIChomozygous108544940
1221646358221646359TC29GENIChomozygous108544942
1221646665221646666CT37GENICpossibly homozygous108544947
1221648600221648601GA34GENIChomozygous109368529
1221650707221650708TC34GENIChomozygous108544961
1221651452221651453TC34GENIChomozygous108544963
1221652266221652267GA31GENIChomozygous109368531
1221652705221652706TC40GENIChomozygous120490594
1221653162221653163CA36GENIChomozygous108544967
1221653197221653198AG36GENIChomozygous108544969
1221654338221654339AG31GENICpossibly homozygous108544971
1221654739221654740CT22GENIChomozygous109368533
1221657029221657030CT23GENIChomozygous108544975
1221657896221657897AG38GENIChomozygous108544977
1221658711221658712TC32GENIChomozygous108544979
1221659740221659741CT21GENIChomozygous109368534
1221660168221660169CT13GENIChomozygous109368536
1221660574221660575TC29GENIChomozygous109368537
1221661142221661143TC30GENIChomozygous108544987
1221661745221661746TC31GENIChomozygous108544991
1221662025221662026TG33GENIChomozygous108544993
1221662902221662903GA43GENIChomozygous108544995
1221663730221663731TC21GENIChomozygous108544997
1221666310221666311GA24GENIChomozygous109368539
1221666627221666628TC25GENIChomozygous109368540
1221666736221666737TG23GENIChomozygous108544999