chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191086188710861888TC13GENIChomozygous109994166
191086193110861932GA8GENIChomozygous109994168
191086339810863399AG23GENIChomozygous109635164
191086428110864282GA17GENIChomozygous109635166
191086526110865262CT19GENIChomozygous109635168
191086574510865746TC12GENIChomozygous109635170
191086575610865757TC16GENIChomozygous109635172
191086580210865803TC29GENIChomozygous109635174
191086646110866462GT16GENIChomozygous110131091
191086721110867212GA26GENIChomozygous110131093
191086816610868167TC15GENIChomozygous109635177
191086819510868196CT17GENIChomozygous109635179
191086999010869991CT7GENICheterozygous125309985
191087040310870404CG23GENIChomozygous125237243
191087061410870615AG26GENIChomozygous125237244
191087078810870789CT29GENIChomozygous119596423
191087097810870979TC23GENIChomozygous109635183
191087106910871070TC14GENIChomozygous110131096
191087107310871074CT12GENIChomozygous110131098
191087133510871336CG31GENIChomozygous110076587
191087161510871616GA10GENIChomozygous110099039