chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12089025220890253GA31GENIChomozygous108834779
12089032620890327GC25GENIChomozygous108834780
12092948220929483TC31GENICheterozygous109039967
12092953820929539GA66GENICheterozygous108052788
12092957020929571CT54GENICheterozygous108052789
12092973120929732CT26GENICheterozygous108052792
12092974020929741CT24GENICheterozygous108052793
12093629820936299AT42GENIChomozygous108693198
12094302120943022GT11GENICpossibly homozygous109039968
12094689720946898TC32GENIChomozygous108693227
12095324620953247GA27GENIChomozygous108834786
12095934120959342AG3GENIChomozygous108834787
12096312420963125TA15GENIChomozygous108834788
12096569720965698CT51GENICheterozygous108052796
12096927920969280GA28GENIChomozygous108834789
12097218920972190AC23GENIChomozygous108693321
12097812320978124AG49GENIChomozygous108834790
12098937020989371GA14GENIChomozygous108052797
12098958020989581CA4GENIChomozygous108052798
12100933321009334AC15GENIChomozygous108052799
12105452321054524GT10GENIChomozygous108052804
12105452721054528AT9GENIChomozygous108052805
12105576521055766AC15GENIChomozygous108693433
12106057521060576TC31GENIChomozygous108052806