chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
380113128011313GA21GENIChomozygous136628497
380122338012234AG27GENIChomozygous136628498
380122848012285TC25GENIChomozygous136628499
380127738012774GA20GENIChomozygous136628500
380132338013234CT17GENIChomozygous136628501
380134498013450C5GENIChomozygous136546514
380137418013742TG20GENIChomozygous136628502
380142418014242CT21GENIChomozygous136628503
380143208014321TG20GENIChomozygous136628504
380146618014664GAG7GENIChomozygous136546516
380146948014697GAA9GENIChomozygous136546518
380160578016058CG15GENIChomozygous136628505
380161018016102CT19GENIChomozygous136628506
380167828016783GA16GENIChomozygous136628507
380172428017243AG20GENIChomozygous136628508
380174708017471C25GENIChomozygous136546520
380175618017565AAAT19GENIChomozygous136546521
380185738018574GA18GENIChomozygous136628509
380186848018685TC23GENIChomozygous136628510
380190078019008GT11GENIChomozygous136628511
380194908019491AG18GENIChomozygous136628512
380200328020032A18GENIChomozygous136546522
380205818020582AG14GENIChomozygous136628513
380230578023058GA14GENIChomozygous136628518
380218168021817CT21GENICpossibly homozygous136628514
380221938022194CT11GENICpossibly homozygous136628515
380226098022610AG31GENIChomozygous136628516
380228968022897GA20GENIChomozygous136628517
380235998023600AT24GENIChomozygous136628519
380239658023966GA22GENIChomozygous136628520
380241128024172AGGTCTTTGGCACTTAGAACTGTAATTCTAAATCTAGCCACTTGGCCCAGGAGTCCAAAC18GENIChomozygous136546523
380242368024241GAAAG16GENIChomozygous136546524
380247638024764TC21GENIChomozygous136628521