chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135128102251281023CT36GENIChomozygous980165120
135128164151281642CT16GENIChomozygous980165121
135128454951284550AG49GENIChomozygous980165122
135128462651284627AG42GENICpossibly homozygous980165123
135128502551285026GA40GENIChomozygous980165124
135128665151286652CT36GENIChomozygous980165125
135128968151289682TC28GENIChomozygous980165126
135128968251289683TC28GENIChomozygous980165127
135128981451289815GA46GENIChomozygous980165128
135128989251289893TG39GENIChomozygous980165129
135129055851290559TC52GENIChomozygous980165130
135129418651294187CT77GENIChomozygous980165131
135129593851295939GA11GENIChomozygous980165132
135129869351298694GC53INTERGENIChomozygous980165133
135129869451298695GA52INTERGENIChomozygous980165134
135130005751300058CT28INTERGENIChomozygous980165135
135130059651300597GA21INTERGENIChomozygous980165136
135130369251303693TC43INTERGENIChomozygous980165137
135130411551304116GA5INTERGENIChomozygous980165138