chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2260978934260978935CG34GENICpossibly homozygous110429127
2260978958260978959GT33GENIChomozygous111048169
2260990230260990231GC35GENIChomozygous110429231
2260993924260993925AT41GENIChomozygous111048171
2260994588260994589TC14GENIChomozygous111048173
2260996399260996400GT27GENIChomozygous110429239
2260996517260996518TG32GENIChomozygous110429241
2260996774260996775CT48GENIChomozygous111048175