chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1174562553174562554G16GENIChomozygous141174813
1174562904174562914ATAATTAACT22GENIChomozygous141174814
1174564084174564084A20GENIChomozygous141174815
1174564118174564119GA25GENIChomozygous141277057
1174564361174564362GA16GENIChomozygous141277058
1174566310174566311TC14GENIChomozygous135752097
1174567144174567145TC17GENIChomozygous141277059
1174567187174567199ACATACACACAC13GENIChomozygous141174816
1174567942174567943GC18GENIChomozygous141277060
1174567981174567981T18GENIChomozygous141174817
1174568560174568561GA10GENIChomozygous141277061
1174569642174569643TC23GENIChomozygous141277062
1174570475174570476AC19GENIChomozygous135752098
1174570702174570702A20GENIChomozygous141174818
1174570986174570987AC27GENIChomozygous135752099
1174571751174571752AG22GENIChomozygous141277063
1174572347174572347T13GENIChomozygous141174819
1174572377174572378T16GENIChomozygous141133997
1174573094174573095CG14GENIChomozygous141277064
1174573264174573265AT17GENIChomozygous141277065
1174573272174573273GA14GENIChomozygous141277066
1174573610174573611CT15GENIChomozygous141277067
1174573691174573692CT16GENIChomozygous141277068
1174574158174574159AG13GENIChomozygous141277069
1174574706174574707CT10GENIChomozygous141277070
1174575045174575046CG14GENIChomozygous141277071
1174575280174575281GA16GENIChomozygous135752101
1174567144174567145T17GENICheterozygous402973657
1174568560174568561G10GENICheterozygous402973658