chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3181061303181061304TA13GENICpossibly homozygous57821365
3181061562181061563GA11GENIChomozygous57821367
3181062456181062457G-21GENICpossibly homozygous58760698
3181063984181063985T-8GENIChomozygous57821373
3181064021181064022AG14GENICpossibly homozygous58760700
3181064963181064964CCTCT5GENIChomozygous57821375
3181065145181065146CA11GENICheterozygous57821377
3181068279181068280TC14GENIChomozygous58760703
3181068646181068647AG20GENIChomozygous57821383
3181069553181069554GC24GENIChomozygous57821387
3181070612181070613AG9GENIChomozygous57821389
3181071294181071295CT26GENIChomozygous57821391
3181071452181071453GA11GENIChomozygous57821393
3181072432181072433T-3GENIChomozygous57821397
3181075084181075087AGG---6GENICheterozygous57821403
3181076360181076361AG20GENIChomozygous57821405
3181079486181079487AAT2GENIChomozygous57821409
3181079710181079711T-2GENIChomozygous58050800