chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171437013314370134TC43GENICheterozygous119266110
171437018314370184TG59GENICheterozygous119266111
171437022114370222CT66GENICheterozygous119266112
171437022414370225GA67GENICheterozygous119266113
171437058114370582TC32GENIChomozygous119266115
171437101814371019GA37GENICheterozygous119266117
171437102514371026CA20GENIChomozygous119266118
171437102614371027TG20GENIChomozygous119266119
171437116614371167CT57GENICheterozygous119266125
171437118014371181CA56GENICheterozygous119266126
171437119914371200CT60GENICheterozygous119266127
171437120514371206GA58GENICheterozygous119266128
171437121814371219CT55GENICheterozygous119266129
171437125514371256TC57GENICheterozygous119266130
171437128014371281GT50GENICheterozygous119266131
171437132514371326TC48GENICheterozygous119266132