chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71204416312044165TT18GENIChomozygous128435625
71204444112044442TC15GENIChomozygous115569442
71204506312045064CG21GENIChomozygous115569443
71204509412045096TT26GENIChomozygous128435626
71204525212045253AG21GENIChomozygous115569444
71204557012045582TGGGTGGATGGG12GENIChomozygous128435627
71204654112046542CT28GENIChomozygous115569446
71204793712047938CG22GENIChomozygous115569447
71204800312048004G22GENIChomozygous128435628
71204929412049295CT19GENIChomozygous115569448
71204934712049347TG21GENIChomozygous128435629
71205029612050297TC24GENIChomozygous115569449
71205069212050693TG23GENIChomozygous115569450
71205069312050694TA24GENIChomozygous115569451
71205079612050796TCTTAT26GENIChomozygous128435630
71205126012051261CT25GENIChomozygous115569452
71205148112051482TC13GENIChomozygous115569453
71205387112053872AT17GENIChomozygous115569458
71205398712053988AG21GENIChomozygous115569459
71205444012054441GA20GENIChomozygous115569460
71205527612055277AG17GENIChomozygous115569462
71205536412055365CT18GENIChomozygous115569463
71205580412055805CT27GENIChomozygous115569464
71205654512056546TG11GENIChomozygous115569465
71205682112056822AT26GENIChomozygous115569466
71205742512057426GA18GENIChomozygous115569467
71205751112057512T20GENICpossibly homozygous128435632
71205876512058766AG21GENIChomozygous115569468
71205915112059152TC21GENIChomozygous115569469
71205947312059474TA15GENIChomozygous115569470
71206033412060334C6GENIChomozygous128435633
71206080012060801TC16GENIChomozygous115569471
71206162912061630AG18GENIChomozygous115569472
71206213312062134TC13GENIChomozygous115569473