chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3181061303181061304TA29GENIChomozygous57821365
3181061562181061563GA34GENIChomozygous57821367
3181062648181062649CT28GENIChomozygous58266626
3181063984181063985T-30GENIChomozygous57821373
3181064963181064964CCTCT29GENIChomozygous57821375
3181065145181065146CA30GENIChomozygous57821377
3181068646181068647AG23GENIChomozygous57821383
3181069553181069554GC24GENIChomozygous57821387
3181070612181070613AG35GENIChomozygous57821389
3181071294181071295CT23GENIChomozygous57821391
3181071452181071453GA23GENICpossibly homozygous57821393
3181071748181071749TG16GENIChomozygous57821395
3181072432181072433T-15GENIChomozygous57821397
3181074816181074817AAGTGTGTGTGT10GENIChomozygous57821401
3181075084181075087AGG---20GENIChomozygous57821403
3181076360181076361AG22GENIChomozygous57821405
3181079486181079487AAT34GENIChomozygous57821409
3181079710181079711T-30GENIChomozygous58050800
3181079740181079741GA38GENICpossibly homozygous58266632
3181065908181065916CACACACA--------9GENIChomozygous58635166