chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3181061303181061304TA37GENIChomozygous57821365
3181061562181061563GA24GENIChomozygous57821367
3181062082181062083CT44GENIChomozygous57821369
3181062336181062337TG28GENIChomozygous57821371
3181063984181063985T-20GENIChomozygous57821373
3181064963181064964CCTCT30GENIChomozygous57821375
3181065145181065146CA37GENIChomozygous57821377
3181065902181065916CACACACACACACA--------------6GENICheterozygous58813432
3181068646181068647AG27GENIChomozygous57821383
3181069185181069186TTA18GENICpossibly homozygous57821385
3181069553181069554GC30GENIChomozygous57821387
3181070612181070613AG37GENIChomozygous57821389
3181071294181071295CT38GENIChomozygous57821391
3181071452181071453GA25GENIChomozygous57821393
3181071748181071749TG31GENIChomozygous57821395
3181072432181072433T-25GENIChomozygous57821397
3181073637181073638TC27GENIChomozygous57821399
3181074816181074817AAGTGTGTGTGT13GENICheterozygous57821401
3181075084181075087AGG---23GENIChomozygous57821403
3181076360181076361AG25GENIChomozygous57821405
3181079486181079487AAT26GENIChomozygous57821409
3181079710181079711T-18GENIChomozygous58050800
3181065906181065916CACACACACA----------6GENICheterozygous58635165
3181074816181074817AAGTGTGTGTGTGT13GENICheterozygous59052286