chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242599697242599698GT33GENICpossibly homozygous108592823
1242602680242602681GT33GENICpossibly homozygous108592824
1242673841242673842AT32GENICheterozygous108592825
1242673849242673850TC39GENICheterozygous108592826
1242673907242673908GA63GENICheterozygous108592827
1242673912242673913CA63GENICheterozygous108592828
1242673918242673919CT73GENICheterozygous108592829
1242673926242673927CG72GENICheterozygous108592830
1242673941242673942TG70GENICheterozygous108592831
1242673958242673959GA70GENICheterozygous108592832
1242673971242673972GA70GENICheterozygous108592833
1242676598242676599CT98GENICheterozygous108592834
1242676600242676601CG96GENICheterozygous108592835
1242676612242676613AT94GENICheterozygous108592836
1242676678242676679GT57GENICheterozygous108592837
1242676682242676683AC68GENICheterozygous108592838
1242677540242677541AC32GENICheterozygous108592839
1242677588242677589CG21GENICheterozygous108592840
1242677619242677620CT20GENICheterozygous108592841
1242677985242677986CT125GENICheterozygous108592842
1242677994242677995AC118GENICheterozygous108592843
1242678005242678006CT120GENICheterozygous108592844
1242713045242713046TC19GENIChomozygous108592845
1242764502242764503TG19GENIChomozygous108592846