chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138828851288288513GA13GENIChomozygous49852408
138828869388288694AG21GENIChomozygous49852409
138828896088288961GA21GENIChomozygous49852410
138828949288289493GC19GENICheterozygous49852411
138829157588291584CAGCCAGAG---------3GENIChomozygous49852420
138829298288292983T-11GENIChomozygous49852433
138829329988293300TC24GENICpossibly homozygous49852434
138829338488293385TC17GENICpossibly homozygous49852435
138829391488293915GA16GENIChomozygous49852436
138829472388294724AG13GENIChomozygous49852437
138829480288294803GA13GENICheterozygous49852438
138829558788295588TC9GENIChomozygous49852439
138829622488296225CT17GENICpossibly homozygous49852447
138829633088296331GT13GENIChomozygous49852448
138829871788298718TA16GENICpossibly homozygous49852450
138829880888298809GA11GENIChomozygous49852451
138829936688299367GA15GENIChomozygous49852458
138829940388299404CCATAGGCTTGTCCATATAGGCTTGTCCAT5GENIChomozygous50497059
138829945788299458GA23GENIChomozygous49852459
138829972588299726GT18GENIChomozygous49852460
138830022688300227GA37GENIChomozygous49852461
138830036888300369TC25GENICpossibly homozygous49852462
138830053788300538AG28GENICpossibly homozygous49852463
138830113488301135GA18GENICpossibly homozygous49852464
138830239088302391GA23GENIChomozygous49852474
138830273588302741TGCTGC------5GENIChomozygous50528890
138830364988303650GA26GENIChomozygous49852476
138830539588305396A-9GENICpossibly homozygous49852477
138830578888305789TC18GENIChomozygous49852478
138830621888306219GA14GENIChomozygous49852479
138830659988306600A-27GENIChomozygous49852480
138830674488306745AG29GENICpossibly homozygous49852481
138830718788307188CT26GENICpossibly homozygous49852482
138830749388307494CT20GENICpossibly homozygous49852483