chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2181530073181530074CT13GENIChomozygous110156644
2181530265181530266AG10GENIChomozygous110156645
2181530478181530479AC13GENIChomozygous110156646
2181532107181532108CT12GENIChomozygous110156649
2181532760181532761TG7GENICheterozygous125598145
2181533330181533331AT21GENIChomozygous110156650
2181533904181533905AT9GENIChomozygous110156651
2181533915181533916CT6GENIChomozygous125598146
2181534986181534987CA17GENIChomozygous110156652
2181535094181535095GA21GENIChomozygous110156653
2181536539181536540CA20GENIChomozygous110156654
2181537069181537070GA11GENIChomozygous110156655
2181537306181537307GA22GENIChomozygous110156656
2181537712181537713CT18GENIChomozygous110156657