chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1248295859248295860CG59GENICpossibly homozygous108604013
1248295862248295863CT58GENICpossibly homozygous108604014
1248297193248297194GT68GENICpossibly homozygous108775890
1248298512248298513AG39GENIChomozygous108604018
1248300374248300375CT56GENIChomozygous108775891
1248300596248300597AG40GENICpossibly homozygous108604021
1248301727248301728CT64GENIChomozygous108775892
1248303281248303282GA58GENIChomozygous108775893
1248304879248304880GA69GENICpossibly homozygous108604026
1248305976248305977AG52GENICheterozygous108775894
1248307944248307945TC38GENIChomozygous108604027
1248308804248308805AT74GENIChomozygous108604028
1248311300248311301TC7GENIChomozygous108775895
1248311314248311315AC7GENIChomozygous108604029
1248311765248311766AG83GENICheterozygous108775896
1248312158248312159CT77GENIChomozygous108775897
1248312643248312644AC55GENIChomozygous108604030
1248314671248314672AG73GENIChomozygous108604032
1248315601248315602CT49GENIChomozygous108604033
1248317068248317069AG51GENICpossibly homozygous108604034
1248317141248317142TC51GENIChomozygous108604035
1248317211248317212TA46GENIChomozygous108604036
1248318709248318710GA70GENIChomozygous108604038
1248319012248319013CT70GENIChomozygous108775898