chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167395035073950351GA45GENIChomozygous64951475
167395345973953460CT60GENICheterozygous64584796
167395462973954630AG64GENIChomozygous64951479
167395467873954679TC87GENIChomozygous64951481
167395540173955402GA53GENIChomozygous64951483
167395541973955420TC54GENIChomozygous64951485
167395558073955581AG35GENIChomozygous64584805
167395581873955819AG47GENICpossibly homozygous64951487
167395604273956043CT69GENIChomozygous64951489
167395619273956193CT83GENIChomozygous64951491
167395637873956379GA29GENIChomozygous64951493
167395668973956690AG27GENIChomozygous64951495
167395805973958060TC34GENIChomozygous64951497
167395874873958749AG30GENIChomozygous64584811
167396075173960752AG18GENIChomozygous64951499
167396371873963719AG32GENIChomozygous64584822
167396799273967993CT20GENIChomozygous64951501
167396859973968600CT24GENIChomozygous64951503
167396872873968729CA45GENIChomozygous64951505
167396890173968902AG26GENIChomozygous64584840