chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71204416312044165TT60GENIChomozygous128435625
71204444112044442TC53GENIChomozygous115569442
71204506312045064CG44GENIChomozygous115569443
71204509412045096TT41GENIChomozygous128435626
71204525212045253AG56GENIChomozygous115569444
71204557012045582TGGGTGGATGGG15GENIChomozygous128435627
71204654112046542CT58GENIChomozygous115569446
71204793712047938CG42GENIChomozygous115569447
71204800312048004G38GENIChomozygous128435628
71204929412049295CT71GENIChomozygous115569448
71204934712049347TG71GENICpossibly homozygous128435629
71205029612050297TC48GENIChomozygous115569449
71205069212050693TG47GENIChomozygous115569450
71205069312050694TA46GENIChomozygous115569451
71205079612050796TCTTAT49GENIChomozygous128435630
71205126012051261CT47GENIChomozygous115569452
71205148112051482TC41GENIChomozygous115569453
71205176712051768GA6GENIChomozygous115569454
71205177112051772GA5GENIChomozygous115569455
71205177712051778G4GENIChomozygous129935469
71205208012052081GA4GENIChomozygous131876562
71205387112053872AT59GENIChomozygous115569458
71205398712053988AG49GENIChomozygous115569459
71205444012054441GA51GENIChomozygous115569460
71205527612055277AG54GENIChomozygous115569462
71205536412055365CT57GENIChomozygous115569463
71205580412055805CT52GENIChomozygous115569464
71205654512056546TG42GENICpossibly homozygous115569465
71205682112056822AT40GENIChomozygous115569466
71205742512057426GA51GENIChomozygous115569467
71205751112057512T53GENIChomozygous128435632
71205876512058766AG62GENIChomozygous115569468
71205915112059152TC49GENIChomozygous115569469
71205947312059474TA37GENIChomozygous115569470
71206033412060334C5GENIChomozygous128435633
71206080012060801TC38GENIChomozygous115569471
71206162912061630AG36GENIChomozygous115569472
71206213312062134TC27GENIChomozygous115569473
71206242812062432AAAG24GENICheterozygous131870164