chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1151627448151627449GC57GENIChomozygous135709415
1151627863151627864CT51GENIChomozygous135709416
1151629172151629173GA64GENIChomozygous143790965
1151629540151629541AG47GENIChomozygous135709417
1151629700151629701GT26GENIChomozygous135709418
1151630110151630111CT20GENIChomozygous135709419
1151630110151630111C20GENICheterozygous403918970
1151630205151630206GA14GENICheterozygous403918971
1151631533151631534AG53GENIChomozygous135709420
1151641488151641489CT53GENIChomozygous135709421
1151644396151644397TA62GENIChomozygous135709422
1151633209151633209ACA50GENICpossibly homozygous135437375
1151630196151630203CACACAC6GENICheterozygous144229249
1151645422151645423AG67GENIChomozygous135709423
1151630205151630206G14GENIChomozygous135437374