chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
711101961110197TC27GENIChomozygous137987345
711108001110801C6GENIChomozygous403198184
711108001110801CA6GENICheterozygous403198185
711119581111959GC25GENIChomozygous137987346
711134211113422TG19GENIChomozygous137987347
711140311114032AG20GENIChomozygous137987348
711149171114918TC22GENIChomozygous137987349
711160221116023AG20GENIChomozygous137987350
711172861117287AC22GENIChomozygous137987351
711185251118526CT9GENIChomozygous137987352
711188751118876TC15GENIChomozygous137987353
711204071120408TC16GENIChomozygous137987354
711205981120599CA26GENIChomozygous137987355
711211731121174TC26GENIChomozygous137987356
711214811121482TC20GENIChomozygous137987357
711223511122352G20GENIChomozygous137932431
711159591115959T11GENICpossibly homozygous137932428
711208071120807CAGA22GENIChomozygous137932429
711208201120822CT26GENIChomozygous137932430
711224871122488CT15GENIChomozygous137987358
711231581123159AG33GENIChomozygous137987359
711234711123472AC13GENIChomozygous154430887
711234711123472AT13GENICheterozygous154430888
711235271123528AG20GENIChomozygous137987360
711244641124465GT11GENIChomozygous137987361
711244661124467AG11GENIChomozygous137987362
711244811124481GATCCGAC15GENIChomozygous137932432
711244821124483TG19GENIChomozygous137987363
711244911124493GT19GENIChomozygous137932433
711244941124494CAC19GENIChomozygous137932434
711248991124900G16GENIChomozygous137932435
711250311125032AC21GENIChomozygous137987364
711251591125160CT27GENIChomozygous137987365
711255821125582AAAC10GENIChomozygous137932436
711257661125767TC18GENIChomozygous137987366
711264031126404GA20GENIChomozygous137987367
711269541126955CT18GENIChomozygous137987368
711274721127473AG24GENIChomozygous137987369
711278091127810TC18GENIChomozygous137987370
711283351128336CG21GENIChomozygous137987371