chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122676149926761500CT6GENIChomozygous50440015
122676229426762295CT13GENICheterozygous50150234
122676235126762352TG8GENIChomozygous50150236
122676235826762363GGCCT-----7GENICpossibly homozygous50150238
122676240326762404TC9GENIChomozygous50150240
122676250426762505AG21GENICpossibly homozygous50299998
122676279326762794AC16GENICpossibly homozygous50300001
122676301726763018AG12GENICheterozygous50440017
122676301826763019TC12GENICheterozygous50300005