chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36647872266478725GAG---6GENICheterozygous57417317
36647964566479646TA22GENICheterozygous57417319
36647986066479861CCA8GENIChomozygous57417321
36648590266485903CT23GENIChomozygous57417327
36648608766486088AG16GENIChomozygous57417329
36648668566486686CT13GENICpossibly homozygous57417331
36648738466487385A-9GENICpossibly homozygous57417333
36648850966488510CT10GENIChomozygous57417335
36649116066491161CA17GENIChomozygous57417341
36649342666493427T-9GENIChomozygous57417343
36649370066493701CG8GENIChomozygous57417345
36649377966493780AAT9GENICheterozygous57417347
36649431466494315GC21GENIChomozygous57417349
36649751166497515ACAC----6GENICheterozygous58687406
36649821666498217AG19GENICpossibly homozygous57417359
36649961066499612TG--5GENIChomozygous57893320
36650020666500207A-2GENIChomozygous57417361
36650061066500611GC10GENIChomozygous57417363
36650142866501429GA15GENICpossibly homozygous57417375
36650147966501480AT6GENICheterozygous57417377
36650255966502560CG9GENIChomozygous57417383
36650258166502582AG21GENICpossibly homozygous57417385
36650264966502650GGC12GENIChomozygous57417387
36650303366503034AG26GENIChomozygous57417389
36650309966503100GA23GENICheterozygous57417391
36650340366503404AG11GENICpossibly homozygous57417392
36650344166503442CT14GENICpossibly homozygous57417394
36650358066503581GA22GENIChomozygous57417396
36650363966503640CT16GENIChomozygous57417398
36650365666503657CT20GENICpossibly homozygous57417400
36650401366504014AG16GENIChomozygous57417402
36650534966505350CT15GENICpossibly homozygous57417404
36650545866505459GT14GENICpossibly homozygous57417406
36650579166505792AG24GENIChomozygous57417408
36650601966506020GA23GENICpossibly homozygous57417410
36650744566507446GA19GENIChomozygous57417412