chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108711712587117126CT21GENIChomozygous950579600
108711756287117563CT17GENIChomozygous950579601
108711810987118110TG9GENIChomozygous950579602
108711836487118365AG9GENIChomozygous950579603
108711912187119122CT25GENIChomozygous950579604
108711931787119318AG18GENIChomozygous950579605
108711972587119726CG16GENIChomozygous950579606
108712033387120334CT13GENIChomozygous950579607
108712096087120961CT9GENIChomozygous950579608
108712118587121186CT8GENIChomozygous950579609
108712176187121762AT17GENIChomozygous950579610
108712191187121912TC27GENIChomozygous950579611
108712199887121999CG21GENIChomozygous950579612
108712229387122294GA23GENIChomozygous950579613
108712241387122414GA18GENIChomozygous950579614
108712350687123507TC11GENIChomozygous950579615
108712379987123800AT18GENIChomozygous950579616
108712427187124272GC27GENIChomozygous950579617
108712475387124754AG33GENIChomozygous950579618
108712519387125194AC22GENIChomozygous950579619
108712555187125552GC23GENIChomozygous950579620
108712578087125781CT14GENIChomozygous950579621
108712609387126094CT24GENIChomozygous950579622
108712640387126404CT17GENIChomozygous950579623
108712666287126663TG20GENIChomozygous950579624
108712691187126912TC17GENIChomozygous950579625
108712722187127222TG5GENIChomozygous950579626
108713054887130549CA21GENICpossibly homozygous950579627
108713235087132351AG25GENIChomozygous950579628
108713357387133574GT28GENIChomozygous950579629
108713409587134096AG20GENIChomozygous950579630
108713537187135372AC16GENIChomozygous950579631
108713847987138480TC6GENIChomozygous950579632