chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32152793021527930T55GENIChomozygous136551861
32152809221528093CT62GENIChomozygous136653674
32152820021528201TG54GENIChomozygous136653675
32152877321528774TC40GENIChomozygous136653676
32152886021528861GC20GENIChomozygous403059145
32152885621528857G8GENICheterozygous404411602
32152885621528857GC8GENIChomozygous404411603
32152886021528861G20GENICheterozygous403059144
32152890221528902AGCAA15GENICpossibly homozygous136551862
32153076121530762AG66GENIChomozygous136653677
32153161521531616CT32GENIChomozygous136653678
32153180521531806CT32GENIChomozygous136653679
32153187821531879AT36GENICpossibly homozygous136653680
32153225221532253TC54GENIChomozygous136653681
32153232621532327CA45GENIChomozygous136653682
32153270821532709TC53GENIChomozygous136653683
32153304321533044AC54GENIChomozygous136653684
32153323021533230T55GENIChomozygous136551863
32153382121533822AG63GENIChomozygous136653685