chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3118095035118095036G-32GENIChomozygous57622713
3118097955118097956A-2GENIChomozygous57622715
3118097973118097974G-2GENIChomozygous57622717
3118097975118097976A-4GENICheterozygous57622719
3118097995118097996CT10GENICpossibly homozygous57622721
3118098002118098003C-9GENIChomozygous57622723
3118098015118098016CA12GENIChomozygous57622725
3118098017118098018AAG12GENICpossibly homozygous57622727
3118098021118098022C-14GENIChomozygous57622729
3118098023118098024C-14GENIChomozygous57622731
3118099404118099405GT52GENIChomozygous57622733
3118101981118101982TG52GENIChomozygous57622735