chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5139647803139647804GT33GENICheterozygous58318080
5139647809139647810GC31GENICheterozygous58318082
5139647815139647816AC27GENICheterozygous58318085
5139656030139656031GT10GENICheterozygous58208787
5139656031139656032TG10GENICheterozygous58208790
5139656032139656033GT10GENICheterozygous58208793
5139656042139656043G-11GENICheterozygous55750118
5139656055139656056G-11GENICheterozygous55750119
5139656089139656090CT8GENICheterozygous55750120
5139656095139656096GT8GENICheterozygous55750121
5139656099139656100TG8GENICheterozygous55750122
5139656129139656130A-7GENICheterozygous55750123
5139656153139656154AC8GENICheterozygous55750124
5139656167139656168CT11GENICheterozygous55750125
5139656172139656173AT11GENICheterozygous55750126
5139656573139656574G-13GENICheterozygous55750127