chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
24923295849232959T-24GENICpossibly homozygous58810108
24923320749233208AT50GENIChomozygous58810110
24923348249233483A-48GENIChomozygous58810112
24923566949235670CT47GENIChomozygous58810114
24923838949238391TG--9GENICpossibly homozygous58810116
24923879849238800TT--36GENIChomozygous58810118
24923922949239230CA15GENICpossibly homozygous58810120
24923999749239998CA42GENIChomozygous58810122
24924009349240094C-12GENIChomozygous58810124
24924024049240241T-9GENIChomozygous58810126
24924049249240493AG28GENICheterozygous58810128
24924049949240500AG29GENICheterozygous58810130
24924051749240518TA22GENICheterozygous58810132
24924052449240525GC20GENICheterozygous58810134
24924057549240576CG46GENICheterozygous58810136
24924068449240685AT15GENICheterozygous58810138
24924261449242615GA71GENICheterozygous58810140
24924303849243039TC28GENICpossibly homozygous58810142
24924333349243334T-16GENIChomozygous58810144
24924334549243346CCCCCA16GENIChomozygous58810146
24924334649243347CCCCA16GENIChomozygous58810148
24924370249243703CT50GENIChomozygous58810150
24924571049245711AG34GENIChomozygous58810158
24924396149243962AATTTTG25GENIChomozygous58810152
24924481849244819AG53GENIChomozygous58810154
24924566349245664A-28GENIChomozygous58810156
24924609249246093AAC22GENIChomozygous58810160