chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101808181218081812G20GENIChomozygous134851709
101808235218082352G18GENIChomozygous131463887
101808237218082372C17GENIChomozygous132143654
101808257818082578TAACCTAGG21GENIChomozygous128792552
101808372318083723A25GENIChomozygous132143655
101808542418085424CAAACT22GENIChomozygous128792555
101808554318085543A21GENIChomozygous128792556
101808557818085579G20GENIChomozygous128792557
101808558318085583A21GENIChomozygous128792558
101808558718085588A20GENIChomozygous128792559
101808559318085593A21GENIChomozygous128792560
101808600718086008TC22GENIChomozygous116502037
101808690818086909AG16GENIChomozygous116502047
101808711718087119AC24GENIChomozygous128792565
101808470618084707GA30GENIChomozygous116740410
101808613918086140GA30GENIChomozygous116740411
101808643718086438GA18GENIChomozygous116740412
101808756418087565CT21GENIChomozygous116502063
101808756418087564A21GENIChomozygous128792566
101808774418087745GT22GENIChomozygous116740413
101808779518087796TC27GENIChomozygous116502071
101808797418087975T19GENIChomozygous128792567
101808824118088242AG26GENIChomozygous116740414
101809046618090467AG15GENIChomozygous116740415