chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261833899261833900AT22GENIChomozygous108630093
1261835253261835254CT46GENIChomozygous108630094
1261836375261836376GA39GENICpossibly homozygous108630095
1261837425261837426AG51GENIChomozygous108630096
1261840651261840652GA64GENIChomozygous108630097
1261841495261841496CT43GENIChomozygous108630098
1261842757261842758TC56GENIChomozygous108630099
1261842876261842877CT60GENIChomozygous108630100
1261844246261844247GA38GENIChomozygous108630101
1261844412261844413GT48GENIChomozygous108630102
1261844541261844542GA46GENIChomozygous108630103
1261845377261845378TC23GENICpossibly homozygous108630104
1261845379261845380TC23GENICpossibly homozygous108630105
1261845381261845382TC23GENICpossibly homozygous108630106
1261848342261848343GA45GENIChomozygous108630107
1261849048261849049AT39GENIChomozygous108630108
1261849051261849052AT37GENIChomozygous108630109
1261849670261849671CT49GENIChomozygous108630110