chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207109141207109142CT12GENIChomozygous110216827
2207109348207109349TA18GENIChomozygous110216828
2207109621207109622CT17GENIChomozygous110216829
2207110269207110270GA23GENIChomozygous110216830
2207111202207111203CG23GENIChomozygous110216831
2207112290207112291AC17GENIChomozygous110216832
2207112908207112909AT23GENIChomozygous110216833
2207114128207114129AT38GENIChomozygous110216834
2207114432207114433GA21GENIChomozygous110216835
2207114788207114789GA21GENIChomozygous110216836
2207117788207117789CA29GENIChomozygous110216838
2207117813207117814AT23GENIChomozygous110216839
2207119499207119500AG23GENIChomozygous110216841
2207119638207119639GC21GENIChomozygous110216842
2207119697207119698GA25GENIChomozygous110216843
2207120959207120960CA22GENIChomozygous110216844
2207122149207122150CT23GENIChomozygous110216845
2207124047207124048AT25GENIChomozygous110216846
2207124242207124243AG21GENIChomozygous110216847
2207126466207126467AT23GENIChomozygous110216848
2207127034207127035TG39GENIChomozygous110216849
2207127361207127362GA29GENIChomozygous110216850
2207127605207127606AG25GENIChomozygous110216852
2207128428207128429CT28GENIChomozygous110216853
2207128966207128967GA32GENIChomozygous110216854
2207129017207129018CT36GENIChomozygous110216855
2207129020207129021AG35GENIChomozygous110216856
2207129243207129244GT23GENIChomozygous110216857
2207120775207120776TA16GENIChomozygous120130372
2207122804207122805CG20GENIChomozygous110620304
2207122805207122806AC20GENIChomozygous110620306