chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167395035073950351GA40GENIChomozygous64951475
167395462973954630AG62GENIChomozygous64951479
167395512673955127GA21GENIChomozygous64584802
167395540173955402GA49GENIChomozygous64951483
167395541973955420TC48GENIChomozygous64951485
167395558073955581AG34GENIChomozygous64584805
167395581873955819AG48GENICpossibly homozygous64951487
167395604273956043CT63GENIChomozygous64951489
167395637873956379GA27GENIChomozygous64951493
167395668973956690AG25GENIChomozygous64951495
167395805973958060TC33GENIChomozygous64951497
167395874873958749AG30GENIChomozygous64584811
167396075173960752AG19GENIChomozygous64951499
167396371873963719AG34GENIChomozygous64584822
167395322873953229GA20GENICheterozygous65008140
167396418273964183CG3GENIChomozygous64774582
167396553973965540AG5GENIChomozygous64774590
167396704173967042CT34GENIChomozygous64584834
167396799273967993CT19GENIChomozygous64951501
167396859973968600CT24GENIChomozygous64951503
167396872873968729CA39GENIChomozygous64951505
167396890173968902AG11GENIChomozygous64584840