chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32313369023133691AG13GENIChomozygous111506035
32313404823134049GA15GENIChomozygous111506036
32313409923134100TC6GENIChomozygous111506037
32313660923136610AG36GENICheterozygous111506038
32313661223136613TC40GENICheterozygous111506039
32313662623136627CA43GENICheterozygous111506040
32313663223136633AG42GENICheterozygous111506041
32313758523137586TC30GENIChomozygous111506042
32313887823138879GA12GENIChomozygous111506043
32313929223139293TC21GENIChomozygous111506044
32314201623142017GA21GENIChomozygous111506045
32314248723142488GA20GENICpossibly homozygous111506046
32314419523144196AC7GENIChomozygous111506047
32314489523144896TA12GENIChomozygous111506048
32314614123146142TC30GENIChomozygous111506049
32314633723146338AG20GENIChomozygous111506050
32314655323146554AG21GENIChomozygous111506051
32314750423147505TC4GENIChomozygous111506052
32314757223147573TG10GENIChomozygous111506053
32314783023147831AG9GENIChomozygous111506054