chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117292549117292550CT28GENIChomozygous115846783
7117294389117294390TG23GENIChomozygous115846785
7117295712117295713CT23GENIChomozygous115846787
7117296103117296104TC17GENIChomozygous115846789
7117296119117296120AG16GENIChomozygous115846791
7117296232117296233GA16GENIChomozygous115846793
7117296630117296631GA31GENIChomozygous115846795
7117297385117297386TA25GENIChomozygous115846797
7117297386117297387TA26GENIChomozygous115846799
7117297425117297426TC21GENIChomozygous115846801
7117297613117297614CG36GENIChomozygous115846803
7117298378117298379AG31GENIChomozygous115846805
7117298438117298439AG27GENIChomozygous115846807
7117299273117299274TC45GENIChomozygous115846809
7117299526117299527AG38GENIChomozygous115846811
7117300366117300367TC22GENIChomozygous115846813