chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167395035073950351GA21GENIChomozygous64951475
167395345973953460CT19GENICheterozygous64584796
167395462973954630AG22GENIChomozygous64951479
167395467873954679TC19GENIChomozygous64951481
167395540173955402GA13GENIChomozygous64951483
167395541973955420TC17GENIChomozygous64951485
167395558073955581AG29GENIChomozygous64584805
167395581873955819AG18GENIChomozygous64951487
167395604273956043CT36GENIChomozygous64951489
167395619273956193CT22GENIChomozygous64951491
167395637873956379GA19GENICpossibly homozygous64951493
167395668973956690AG30GENIChomozygous64951495
167395805973958060TC19GENIChomozygous64951497
167395874873958749AG12GENIChomozygous64584811
167396075173960752AG19GENIChomozygous64951499
167396371873963719AG21GENIChomozygous64584822
167396553973965540AG3GENIChomozygous64774590
167396799273967993CT21GENIChomozygous64951501
167396859973968600CT16GENIChomozygous64951503
167396872873968729CA14GENIChomozygous64951505
167396890173968902AG11GENIChomozygous64584840