chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72354609523546096AC12GENIChomozygous115616290
72354651023546511CA15GENIChomozygous115616291
72354668723546688AG17GENIChomozygous115616292
72354713323547134CG19GENIChomozygous115616293
72354832023548321CT16GENIChomozygous115616294
72354849223548493TC21GENIChomozygous115616295
72355342223553423TC22GENIChomozygous115616297
72357439423574395CT28GENIChomozygous115616299
72357647523576476CT23GENIChomozygous115616300
72357679423576795CT8GENIChomozygous115616301
72357866623578667AG37GENIChomozygous115616305
72357962423579625CG28GENIChomozygous115616306
72358214023582141CT20GENIChomozygous115616308
72358236423582365TG25GENIChomozygous115616309
72358330923583310AG28GENIChomozygous115616310
72358426923584270AC20GENIChomozygous115616311
72358495123584952TA23GENIChomozygous115616312
72358737223587373TA29GENIChomozygous115616313
72358831923588320TG11GENIChomozygous115616314
72358832423588325TC10GENIChomozygous115616315
72358834623588347TC10GENIChomozygous115616316
72358837123588372AG15GENIChomozygous115616317
72358837523588376AG16GENIChomozygous115616318
72358868423588685TG11GENIChomozygous115616319
72358942123589422AC9GENIChomozygous115616320
72358942723589428AT6GENIChomozygous115616321
72358961523589616AG5GENICheterozygous116385428
72358979223589793AC4GENIChomozygous115616323
72359004423590045AG22GENIChomozygous115616324
72359260623592607CA20GENIChomozygous115616325
72359382123593822GC13GENIChomozygous115616326