chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8127144599127144600GA11GENIChomozygous116715787
8127144623127144623GG9GENIChomozygous128645942
8127145067127145068T18GENIChomozygous128645943
8127145144127145144C22GENIChomozygous128645947
8127145084127145084A21GENIChomozygous128645944
8127145135127145135A20GENIChomozygous128645945
8127145142127145142GG21GENIChomozygous128645946
8127145155127145155CC24GENIChomozygous128645948
8127145343127145343C15GENIChomozygous128645949
8127145400127145401AC10GENIChomozygous116715793
8127145412127145412G8GENIChomozygous128645950
8127145434127145434C6GENIChomozygous128645951
8127145441127145441C6GENIChomozygous128645952
8127145447127145448T4GENIChomozygous128645953
8127145566127145566G6GENIChomozygous128645957
8127145577127145578T7GENIChomozygous128645958
8127145593127145593C10GENIChomozygous128645959
8127145617127145617A12GENIChomozygous128645960
8127145635127145637CT14GENIChomozygous128645961
8127145662127145663CA14GENICpossibly homozygous116899193
8127145920127145921CG2GENIChomozygous116715797
8127146001127146002A4GENIChomozygous128645962
8127146008127146008G4GENIChomozygous128645963
8127146013127146013G4GENIChomozygous128645964
8127146408127146409GA12GENIChomozygous116715799
8127146767127146768GA8GENIChomozygous116715801
8127147912127147913AG20GENIChomozygous116715805
8127148479127148479T3GENIChomozygous128645966
8127148530127148531C8GENIChomozygous132874854
8127148644127148645TC11GENIChomozygous116715809
8127148787127148788CT16GENIChomozygous116715811
8127149179127149180GC17GENIChomozygous116715813
8127150167127150168AG7GENIChomozygous116715815
8127152351127152352GA12GENIChomozygous116715817
8127152598127152599CG18GENIChomozygous116715819
8127150136127150137AC7GENIChomozygous117921364