chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108396766108396767TC15GENIChomozygous51596096
10108397090108397091GT18GENIChomozygous51596098
10108397871108397872CT15GENIChomozygous51596100
10108397987108397988CT13GENIChomozygous51596102
10108398368108398369AG15GENIChomozygous51596104
10108398613108398614CT14GENIChomozygous53547848
10108398863108398864TC9GENIChomozygous51596106
10108399592108399593CT7GENIChomozygous51596108
10108400449108400450AG10GENIChomozygous51596112
10108401486108401487TC7GENIChomozygous51596116
10108402283108402284AG28GENIChomozygous51596118
10108403550108403551TTAAC11GENIChomozygous51596120
10108403553108403554GGGGCTAC11GENIChomozygous51596122
10108403922108403924AA--17GENIChomozygous51596124
10108405663108405664TTC13GENIChomozygous51596126
10108407879108407880AT12GENIChomozygous51596132
10108408876108408877AT8GENIChomozygous52409531
10108409221108409222TTC18GENICpossibly homozygous53547849
10108409485108409486AG22GENIChomozygous51596140
10108410992108410993CT14GENIChomozygous51772052
10108412065108412066GA12GENIChomozygous51596148
10108412067108412068CCT12GENIChomozygous51596149
10108412524108412525CT15GENIChomozygous51596151
10108412774108412775TC14GENIChomozygous51596153