chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106541600965416010CA30GENIChomozygous51477692
106541605165416052GA30GENIChomozygous51906324
106541615665416157GA29GENIChomozygous51906326
106541617865416179CA31GENIChomozygous51477694
106541618665416187AG30GENIChomozygous51477695
106541621065416211TC29GENIChomozygous51477696
106541637065416371GA20GENIChomozygous51906328
106541647865416479CT24GENIChomozygous51477698
106541647965416480AG24GENIChomozygous51477699
106541648765416488GT26GENIChomozygous51477700
106541648965416490TC26GENIChomozygous51477701
106541660865416609GA18GENIChomozygous51477703
106541664965416650GGTTA26GENIChomozygous51906333
106541665165416652GGAGGGC27GENIChomozygous51906335
106541677165416772CT2GENIChomozygous51477706
106541681665416817AC8GENIChomozygous51906337
106541683965416843TTTG----14GENIChomozygous51906339
106541686965416870GT23GENIChomozygous51906341
106541696365416964GA14GENIChomozygous51477708
106541696965416970AT13GENIChomozygous51477709
106541699665417000CTTC----14GENIChomozygous51477710
106541763265417633GGT12GENICheterozygous51477714
106541763265417633GGTT12GENICheterozygous52382158
106541628965416291TG--19GENIChomozygous52320241
106541629065416291GGCCA19GENIChomozygous52320243
106541698065416981TA11GENIChomozygous52382152
106541698165416982CA10GENIChomozygous52382154
106541698265416983TG10GENIChomozygous52382156
106541776365417764CG27GENIChomozygous51477717
106541776465417765TC27GENIChomozygous51477718
106541791965417920AG22GENIChomozygous51477721
106541815465418156TG--14GENICpossibly homozygous52382160
106541816065418161GGGTTT14GENICpossibly homozygous52382162
106541818565418186CCT13GENIChomozygous51477726
106541847665418477GT30GENIChomozygous51906345
106541860865418609AG24GENIChomozygous51477728
106541875465418755CA24GENIChomozygous51906347
106541876365418764AC29GENIChomozygous51477730
106541881665418817GA24GENIChomozygous51906349
106541882365418824AG25GENIChomozygous51477731