chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120063978120063979AG26GENIChomozygous115854873
7120064432120064433GC29GENIChomozygous115854875
7120064857120064858AG28GENIChomozygous115854877
7120064893120064894TC31GENIChomozygous115854879
7120065209120065210AG28GENIChomozygous115854881
7120065685120065686CA12GENIChomozygous115854883
7120066280120066281GA33GENICpossibly homozygous115854885
7120066676120066677GA42GENIChomozygous115854887
7120066745120066746TG42GENIChomozygous115854889
7120066792120066793CG36GENIChomozygous115854891
7120067036120067037TC20GENIChomozygous115854893
7120067349120067350CT26GENIChomozygous115854895
7120070312120070313TC27GENIChomozygous115854897