chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230967097230967097TTTTTTTTTTTTTTATT2GENIChomozygous140970827
2230971744230971745CA20GENICpossibly homozygous136502719
2230971778230971788CACACCCACT22GENICheterozygous141086555
2231036161231036162CG59GENIChomozygous136502834
2231036587231036588CG68GENIChomozygous146689783
2231038354231038355CG53GENICpossibly homozygous153943222
2231051977231051978TA57GENIChomozygous136502847
2231059192231059193GA73GENICpossibly homozygous145383921
2231062219231062220GT51GENIChomozygous136502860
2231073001231073003AG50GENIChomozygous140970828
2231073016231073016A49GENIChomozygous140970829
2231089927231089928A11GENICheterozygous135987444
2231089927231089928AG11GENICheterozygous403043827
2231108285231108286TC8GENICheterozygous403043830
2231108285231108286T8GENICpossibly homozygous403043831
2231108285231108286TG8GENICheterozygous403043832
2231111589231111589GGGATG26GENIChomozygous135987448
2231110936231110938AC19GENICheterozygous146644834
2231108292231108293TC10GENICheterozygous136502886
2231038354231038355C53GENICheterozygous403709163
2231073009231073010GA50GENIChomozygous140984087
2231073025231073026GA46GENIChomozygous140984088
2231073040231073041AG46GENIChomozygous140984089
2231073177231073185AGAAGAAG13GENIChomozygous148285432
2231089926231089926GG12GENICheterozygous145202569