chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137025966370259664TC50GENIChomozygous809095616
137026731570267316CT46GENIChomozygous809095617
137026814470268145GA56GENIChomozygous809095618
137026850270268503CA50GENIChomozygous809095619
137027172870271729TC20GENIChomozygous809095620
137027185070271851TC28GENIChomozygous809095621
137027550870275509AT47GENIChomozygous809095622
137027600370276004GA42GENIChomozygous809095623
137027612970276130TC47GENIChomozygous809095624
137027954770279548TC37GENIChomozygous809095625
137028235070282351CG45GENICpossibly homozygous809095626
137028476270284763CT46GENIChomozygous809095627
137029326670293267CT44GENIChomozygous809095628
137029651570296516CT32GENIChomozygous809095629
137029768370297684CA38GENICheterozygous809095630
137029804070298041AG9GENIChomozygous809095631
137029805270298053AT10GENIChomozygous809095632
137030672170306722TC32GENIChomozygous809095633