chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154891084154891085CT12GENICheterozygous57744439
3154891156154891157TG6GENIChomozygous57744441
3154891329154891330CT16GENICpossibly homozygous57744443
3154892302154892303AG29GENICpossibly homozygous57744445
3154893163154893164TTAC4GENICheterozygous57744447
3154893389154893390TC38GENICpossibly homozygous57744449
3154895801154895802AC8GENIChomozygous57744451