chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4160673500160673501TA18GENIChomozygous57540499
4160674398160674399AC20GENIChomozygous57540501
4160677598160677599AG23GENIChomozygous57540503
4160680641160680642T-12GENIChomozygous57540505
4160681447160681448TTCC2GENIChomozygous57540507
4160681867160681868AG27GENIChomozygous57540509
4160684098160684099TTAAAC25GENIChomozygous57540511
4160684756160684757AG22GENIChomozygous57540513
4160685103160685104CT29GENIChomozygous57540515
4160687902160687913TTTTTTTTTTG-----------16GENIChomozygous57540517
4160687912160687913G-15GENIChomozygous57003239
4160688115160688116AC20GENIChomozygous57540519
4160692565160692566CA15GENIChomozygous57540521
4160697663160697664CA29GENIChomozygous57540523
4160698064160698065TG37GENICheterozygous57540524
4160702176160702177AT20GENIChomozygous57540526
4160705208160705209AG21GENIChomozygous57540528
4160705240160705241CT13GENIChomozygous57540530
4160705321160705322T-14GENIChomozygous57351095
4160708355160708356T-14GENICpossibly homozygous57351097
4160708749160708750T-18GENIChomozygous57540532
4160713148160713149AC37GENIChomozygous57540534
4160716957160716958AC28GENIChomozygous57540536
4160717124160717125TC25GENIChomozygous57540538
4160717127160717128TC25GENIChomozygous57540540
4160717188160717189C-2GENIChomozygous57003244
4160720906160720907T-10GENIChomozygous57003246
4160721103160721104GT27GENIChomozygous57540542
4160721305160721306CT26GENIChomozygous57540544
4160721700160721701TC18GENIChomozygous57540546
4160723151160723152GC26GENIChomozygous57540548
4160723263160723264GA20GENIChomozygous57540550
4160727524160727525CT24GENIChomozygous57540552
4160728022160728023GA31GENIChomozygous57540554
4160728968160728969TTAA7GENICpossibly homozygous57540556
4160728968160728969TTA7GENICheterozygous57540558
4160729859160729860CA19GENIChomozygous57540560
4160729860160729861CG19GENIChomozygous57540562
4160730441160730442AG24GENIChomozygous57540564
4160731364160731365GC30GENIChomozygous57540566
4160732361160732362GA41GENIChomozygous57540568