chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226085439226085440AG39GENICpossibly homozygous510480543
1226085528226085530CA--32GENICpossibly homozygous685165709
1226085589226085590AACG45GENICheterozygous685165710
1226085634226085635TC35GENICheterozygous510480544
1226085662226085663CT17GENICheterozygous510480545
1226086829226086830TA69GENIChomozygous510480546
1226087132226087133G-66GENIChomozygous685165711
1226087314226087315TC38GENICpossibly homozygous507216543
1226087315226087316TC38GENICpossibly homozygous507216544
1226087729226087730CT53GENIChomozygous510480547
1226088742226088743TC57GENIChomozygous507216545