chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2251829633251829634GA28GENICpossibly homozygous111037852
2251829796251829797AG29GENIChomozygous111037854
2251830377251830378CG25GENIChomozygous111037856
2251832603251832604GA27GENIChomozygous111037858
2251833612251833613AT30GENIChomozygous120132172
2251833613251833614TG29GENIChomozygous120132173
2251834843251834844GA26GENIChomozygous111037860
2251835460251835461CT18GENIChomozygous111037862
2251836266251836267GT20GENIChomozygous110386486
2251837738251837739CA18GENICpossibly homozygous111037866