chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32152793021527930T10GENIChomozygous136551861
32152809221528093CT22GENIChomozygous136653674
32152820021528201TG25GENIChomozygous136653675
32152877321528774TC11GENIChomozygous136653676
32152885821528859GC9GENICheterozygous404411605
32152885621528857G7GENICheterozygous404411602
32152885621528857GC7GENICheterozygous404411603
32152885821528859G9GENICheterozygous404411604
32152885421528855GC7GENICpossibly homozygous403059143
32152886021528861G9GENICheterozygous403059144
32152886021528861GC9GENICheterozygous403059145
32152890221528902AGCAA7GENIChomozygous136551862
32153076121530762AG16GENIChomozygous136653677
32153161521531616CT15GENIChomozygous136653678
32153180521531806CT4GENIChomozygous136653679
32153187821531879AT16GENIChomozygous136653680
32153225221532253TC18GENIChomozygous136653681
32153232621532327CA19GENIChomozygous136653682
32153270821532709TC20GENIChomozygous136653683
32153304321533044AC23GENIChomozygous136653684
32153323021533230T12GENIChomozygous136551863
32153382121533822AG19GENIChomozygous136653685
32152885421528855G7GENICheterozygous403059142