chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
67556197775561978TC12GENIChomozygous114861553
67556268675562687TG27GENIChomozygous115124976
67556340775563408AC31GENIChomozygous114861555
67556350075563501GA17GENIChomozygous115124977
67556422375564224AG23GENIChomozygous114861556
67556557175565572CG17GENIChomozygous115124978
67556597475565975CT24GENIChomozygous115124979
67556610575566106GC12GENIChomozygous114861557
67556629275566293TC15GENIChomozygous115124980
67556718775567188AG23GENIChomozygous115124981
67556844075568441GA17GENIChomozygous115124982
67556937075569371GA11GENIChomozygous115124984
67556971575569716GA23GENIChomozygous115124985
67557215375572154GA17GENICpossibly homozygous114861560
67557233575572336CT19GENIChomozygous115124986
67557297275572973AG13GENIChomozygous114861561
67557347475573475GA24GENIChomozygous115124987
67557361275573613CT28GENIChomozygous115124988
67557462375574624AG38GENIChomozygous114861563
67557599275575993CG7GENIChomozygous115124989
67557606975576070AG17GENIChomozygous114861564
67557673775576738GA11GENIChomozygous114861565
67557871275578713CT21GENIChomozygous115124990
67557899675578997TC19GENIChomozygous114861567
67557909175579092GA17GENIChomozygous115124991
67557912375579124GC15GENIChomozygous114861568
67557984675579847AG17GENICpossibly homozygous115124992
67557993075579931GA17GENIChomozygous115124993
67558150675581507CT31GENICheterozygous115215581
67558295375582954CT31GENICheterozygous115124994
67558488775584888AG5GENIChomozygous115125001
67558488975584890TC6GENIChomozygous114861573
67558498575584986CT14GENIChomozygous114861574
67558708375587084AC29GENIChomozygous114861577
67558772775587728GA17GENIChomozygous114861578
67558813975588140AT21GENIChomozygous115125002