chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261833899261833900AT17GENIChomozygous108630093
1261835253261835254CT29GENIChomozygous108630094
1261836375261836376GA16GENIChomozygous108630095
1261837425261837426AG19GENIChomozygous108630096
1261840651261840652GA10GENIChomozygous108630097
1261841495261841496CT11GENIChomozygous108630098
1261842757261842758TC18GENIChomozygous108630099
1261842876261842877CT22GENIChomozygous108630100
1261844246261844247GA16GENIChomozygous108630101
1261844412261844413GT14GENIChomozygous108630102
1261844541261844542GA13GENIChomozygous108630103
1261848342261848343GA12GENIChomozygous108630107
1261849048261849049AT14GENIChomozygous108630108
1261849051261849052AT14GENIChomozygous108630109
1261849670261849671CT8GENIChomozygous108630110