chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118597769985977700CT25GENICpossibly homozygous148083371
118597862885978629TC24GENIChomozygous145769953
118597871985978720GA19GENIChomozygous145769954
118597908885979089AG16GENIChomozygous145769955
118597926085979261GA17GENIChomozygous148083372
118598145285981453GA18GENIChomozygous148083373
118598588885985889GA19GENIChomozygous145769961
118598654985986550GA21GENIChomozygous148083374
118598751685987518AT20GENIChomozygous145754747
118598756285987563AG23GENIChomozygous145769964
118599079785990797TTCCTGGTT20GENIChomozygous145754750
118599158785991588GA16GENIChomozygous145769970
118599191885991919GT22GENIChomozygous148083375
118599218785992188CT24GENIChomozygous148083376
118599348785993488GA20GENIChomozygous148083377
118598186985981869A19GENICpossibly homozygous148068215
118598307085983071AG27GENIChomozygous139034553
118598310085983101TA27GENIChomozygous139034554
118598312385983124AG26GENIChomozygous139034555
118599206085992060AGA27GENIChomozygous138898745
118599653885996539CA15GENIChomozygous139034556
118599040485990405T7GENIChomozygous403902971
118599040485990405TA7GENICheterozygous154725173