chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2138782374138782375CCT18GENICpossibly homozygous59115234
2138782809138782810CA26GENIChomozygous59115236
2138783635138783636TA51GENIChomozygous59115238
2138784616138784617TC33GENIChomozygous59115240
2138786098138786099TC38GENIChomozygous59862787
2138786202138786203AG29GENIChomozygous59862789
2138787346138787347GT29GENICpossibly homozygous59862791