chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108396766108396767TC9GENIChomozygous51596096
10108397090108397091GT21GENIChomozygous51596098
10108397871108397872CT16GENIChomozygous51596100
10108398368108398369AG12GENIChomozygous51596104
10108398863108398864TC16GENIChomozygous51596106
10108399592108399593CT14GENIChomozygous51596108
10108400449108400450AG17GENIChomozygous51596112
10108401486108401487TC6GENIChomozygous51596116
10108402283108402284AG14GENIChomozygous51596118
10108403922108403924AA--20GENIChomozygous51596124
10108405663108405664TTC18GENIChomozygous51596126
10108407879108407880AT14GENIChomozygous51596132
10108408876108408877AT11GENIChomozygous52409531
10108408887108408888TC11GENIChomozygous51953781
10108409485108409486AG19GENIChomozygous51596140
10108410258108410259TA16GENIChomozygous51596142
10108411935108411936CT11GENIChomozygous51596146
10108412065108412066GA11GENIChomozygous51596148
10108412067108412068CCT11GENIChomozygous51596149
10108402257108402258CT19GENIChomozygous52271545
10108402268108402269AT15GENIChomozygous52271547
10108403116108403117AG11GENIChomozygous52271549
10108406307108406308CT18GENIChomozygous52271551
10108406576108406577A-8GENICheterozygous53533266
10108412524108412525CT24GENIChomozygous51596151
10108412774108412775TC23GENIChomozygous51596153