chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9112834235112834236CT21GENIChomozygous52115369
9112835609112835610CT42GENIChomozygous52301500
9112836452112836453AG25GENIChomozygous52115373
9112836769112836770TC35GENIChomozygous52115375
9112837362112837365CCC---3GENICheterozygous52919311
9112837746112837747AG20GENIChomozygous52115379
9112838182112838183AC28GENIChomozygous52115381
9112838256112838257AG30GENIChomozygous52115383
9112840034112840036AA--18GENIChomozygous52919313
9112841036112841037A-22GENIChomozygous52115387
9112842092112842093GA22GENIChomozygous52115389
9112842392112842393AG21GENIChomozygous52115391
9112843084112843085AG15GENIChomozygous52115393
9112843147112843148AAAAAG2GENIChomozygous52959814
9112843647112843658AAAAAAAAAAA-----------16GENICpossibly homozygous52115395
9112845258112845259CCTTTT6GENIChomozygous52115399
9112845274112845279GGGGC-----16GENICpossibly homozygous52959816
9112845792112845793GA20GENIChomozygous52115407
9112846503112846504CCGT29GENIChomozygous52115411
9112848889112848890AG31GENIChomozygous52115413
9112851685112851686A-17GENIChomozygous52301506
9112852639112852641TG--32GENIChomozygous52301508
9112852998112853103AGAAATTGAAACTCGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCAAAAAAAAAAAAAAAAA---------------------------------------------------------------------------------------------------------15GENIChomozygous52919315
9112854063112854064GA27GENIChomozygous52301510
9112854085112854086CG26GENIChomozygous52301512
9112854385112854386CCT21GENIChomozygous52115417
9112857054112857055AG26GENIChomozygous52115421
9112857602112857603TTG25GENIChomozygous52115423
9112857701112857702CG28GENIChomozygous52115425
9112858302112858303AG36GENICpossibly homozygous52115427
9112862813112862814AG19GENIChomozygous52115433
9112863595112863596CA27GENIChomozygous52115437
9112863967112863968AC28GENIChomozygous52115439