chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3181061303181061304TA24GENIChomozygous57821365
3181061562181061563GA36GENIChomozygous57821367
3181062648181062649CT36GENIChomozygous58266626
3181063984181063985T-23GENIChomozygous57821373
3181064963181064964CCTCT27GENIChomozygous57821375
3181065145181065146CA27GENIChomozygous57821377
3181065906181065916CACACACACA----------7GENICheterozygous58635165
3181065908181065916CACACACA--------7GENICpossibly homozygous58635166
3181068646181068647AG32GENIChomozygous57821383
3181069553181069554GC27GENIChomozygous57821387
3181070612181070613AG33GENIChomozygous57821389
3181071294181071295CT34GENIChomozygous57821391
3181071452181071453GA37GENIChomozygous57821393
3181071748181071749TG24GENIChomozygous57821395
3181072432181072433T-25GENIChomozygous57821397
3181074816181074817AAGTGTGTGTGT7GENIChomozygous57821401
3181075084181075087AGG---20GENIChomozygous57821403
3181076360181076361AG22GENIChomozygous57821405
3181078562181078563A-15GENICheterozygous57821407
3181079486181079487AAT24GENIChomozygous57821409
3181079710181079711T-27GENIChomozygous58050800
3181079740181079741GA30GENIChomozygous58266632