chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106541600965416010CA26GENIChomozygous51477692
106541617865416179CA39GENIChomozygous51477694
106541618665416187AG39GENIChomozygous51477695
106541621065416211TC39GENIChomozygous51477696
106541628965416291TG--39GENIChomozygous52320241
106541629065416291GGCCA37GENIChomozygous52320243
106541647865416479CT25GENIChomozygous51477698
106541647965416480AG25GENIChomozygous51477699
106541648765416488GT23GENIChomozygous51477700
106541648965416490TC21GENIChomozygous51477701
106541657765416578AT41GENIChomozygous51477702
106541660865416609GA39GENIChomozygous51477703
106541664965416650GGTTA28GENICheterozygous51906333
106541677165416772CT43GENIChomozygous51477706
106541692865416929TTCTATATAC15GENIChomozygous51477707
106541696365416964GA13GENIChomozygous51477708
106541696965416970AT10GENIChomozygous51477709
106541699665417000CTTC----5GENIChomozygous51477710
106541763265417633GGT25GENICheterozygous51477714
106541763265417633GGTT25GENICpossibly homozygous52382158
106541698065416981TA7GENIChomozygous52382152
106541698165416982CA6GENIChomozygous52382154
106541698265416983TG6GENIChomozygous52382156
106541776365417764CG17GENIChomozygous51477717
106541776465417765TC17GENIChomozygous51477718
106541791965417920AG29GENIChomozygous51477721
106541815465418155TTTTG26GENICheterozygous51477723
106541815465418156TG--33GENICheterozygous52382160
106541815965418161TG--27GENICheterozygous51477725
106541816065418161GGGTTT34GENICheterozygous52382162
106541818565418186CCT32GENICpossibly homozygous51477726
106541860865418609AG41GENIChomozygous51477728
106541872665418727CT40GENICpossibly homozygous51477729
106541875465418755CA17GENICheterozygous51906347
106541876365418764AC17GENIChomozygous51477730
106541882365418824AG26GENIChomozygous51477731
106541915165419152CA37GENIChomozygous51477732