chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3181061303181061304TA11GENIChomozygous57821365
3181061562181061563GA15GENIChomozygous57821367
3181062648181062649CT23GENIChomozygous58266626
3181063984181063985T-18GENIChomozygous57821373
3181064963181064964CCTCT21GENIChomozygous57821375
3181065145181065146CA26GENIChomozygous57821377
3181066105181066106GT9GENIChomozygous57821381
3181068646181068647AG15GENIChomozygous57821383
3181069553181069554GC7GENIChomozygous57821387
3181070612181070613AG19GENIChomozygous57821389
3181071294181071295CT19GENIChomozygous57821391
3181071452181071453GA9GENIChomozygous57821393
3181071748181071749TG18GENIChomozygous57821395
3181072432181072433T-11GENIChomozygous57821397
3181075084181075087AGG---14GENIChomozygous57821403
3181076360181076361AG19GENIChomozygous57821405
3181079486181079487AAT22GENIChomozygous57821409
3181079740181079741GA7GENIChomozygous58266632
3181067223181067224GA7GENIChomozygous60410349