chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3181061303181061304TA58GENIChomozygous57821365
3181061562181061563GA41GENIChomozygous57821367
3181062648181062649CT36GENIChomozygous58266626
3181063984181063985T-31GENIChomozygous57821373
3181064646181064647CA43GENICheterozygous58266628
3181064963181064964CCTCT25GENIChomozygous57821375
3181065145181065146CA62GENIChomozygous57821377
3181065902181065910CACACACA--------3GENIChomozygous57821379
3181066105181066106GT18GENIChomozygous57821381
3181068646181068647AG64GENIChomozygous57821383
3181069553181069554GC42GENIChomozygous57821387
3181070612181070613AG30GENIChomozygous57821389
3181071294181071295CT48GENIChomozygous57821391
3181071452181071453GA47GENIChomozygous57821393
3181071748181071749TG31GENIChomozygous57821395
3181071795181071800TCTTT-----20GENICheterozygous58266630
3181072432181072433T-31GENIChomozygous57821397
3181073402181073403TG44GENICheterozygous58522802
3181074816181074817AAGTGTGTGTGT8GENIChomozygous57821401
3181075084181075087AGG---48GENIChomozygous57821403
3181076360181076361AG45GENIChomozygous57821405
3181078562181078563A-22GENICheterozygous57821407
3181079486181079487AAT48GENIChomozygous57821409
3181079740181079741GA27GENIChomozygous58266632