chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117235115117235116TA74GENIChomozygous119407032
4117235893117235894CT76GENIChomozygous112818337
4117237398117237399TC58GENIChomozygous119407033
4117238977117238977TTAG53GENIChomozygous128072513
4117239405117239406GT8GENIChomozygous112818339
4117241894117241895CT69GENIChomozygous112818343
4117247163117247164GT71GENIChomozygous112818345
4117247408117247409TC62GENIChomozygous119407034
4117247781117247795GCTTTTACCATTGT73GENIChomozygous131360185
4117248423117248424TC74GENIChomozygous112818347
4117251603117251604TC66GENIChomozygous112818349
4117244809117244810AC54GENICpossibly homozygous119527417