chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8114537778114537779CA17GENIChomozygous53166433
8114537901114537902AAT21GENIChomozygous53166435
8114537983114537984AG27GENIChomozygous53166437
8114538548114538551TTT---1GENIChomozygous52824070
8114538605114538606TC11GENICpossibly homozygous52824072
8114538692114538693GA16GENIChomozygous53166439
8114538873114538874AT42GENIChomozygous52824073
8114539861114539862CA34GENIChomozygous52824076
8114541278114541279TTG22GENIChomozygous52824084
8114541912114541913AG20GENIChomozygous52824085
8114542225114542226G-21GENIChomozygous52824086
8114542643114542644GA42GENIChomozygous53166441
8114543333114543334GA32GENIChomozygous53166443