chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124867667948676680GT6GENIChomozygous50228761
124867679248676793AG10GENIChomozygous50228763
124867692248676923GGAAAA5GENIChomozygous50228765
124867733848677339CT10GENIChomozygous50228770
124867796648677967TA14GENIChomozygous50228772
124867816048678164ACAC----13GENICheterozygous50623027
124867816248678164AC--13GENICheterozygous50565940
124867916348679164G-20GENIChomozygous50228774
124867997648679978AA--18GENICheterozygous50513626
124867997748679978A-18GENICpossibly homozygous50513628
124868057148680572GC16GENIChomozygous50228776
124868063248680638TTTTTG------6GENIChomozygous50228778
124868081448680815CCTT10GENICheterozygous50565942
124868083348680835GG--11GENICheterozygous50513630
124868087348680874TC8GENIChomozygous50228788
124868123948681241AG--3GENIChomozygous50615974
124868129948681300C-11GENICheterozygous50615975
124868162248681623CT24GENIChomozygous50228790
124868197348681974CG15GENIChomozygous50228792
124868262048682621CT18GENIChomozygous50228794
124868275148682752TC20GENIChomozygous50228796
124868292048682924GTGT----21GENIChomozygous50228798
124868367248683677TTTTT-----16GENICheterozygous50228800
124868369348683694T-18GENICheterozygous50228802
124868394748683948GA23GENIChomozygous50228804
124868367348683677TTTT----16GENICheterozygous50546429
124868433248684333AAGTGTGT6GENICheterozygous50546430
124868433248684333AAGTGTGTGT6GENICheterozygous50546431
124868480148684828AGATGGATGGAATCCTAACACCTGGAT---------------------------26GENIChomozygous50228806
124868535948685360T-8GENIChomozygous50228808
124868546548685573AGTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCG------------------------------------------------------------------------------------------------------------12GENIChomozygous50513632
124868615448686155TC22GENIChomozygous50228818
124868646448686465AG19GENIChomozygous50228820
124868653948686540GA30GENIChomozygous50228822
124868769248687693TC24GENIChomozygous50228824