chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152473512024735123TTT---8GENIChomozygous48479680
152473516024735161CCTTTTTTTCT6GENIChomozygous48479685
152473524024735264TGTGTGTGTGTGTGTGTGTGTGTG------------------------11GENIChomozygous48479687
152473554624735547CT58GENIChomozygous48479689
152473591624735917TC45GENIChomozygous48479691
152473633924736340CT27GENIChomozygous48479693
152473692224736923TC53GENIChomozygous48479695
152473992324739924GA25GENIChomozygous48479701
152474001224740013AT25GENIChomozygous48479703
152474444524744446AAAAAC20GENIChomozygous48479707
152474483724744838AG29GENIChomozygous48479709
152474564624745647CCAAA1GENIChomozygous49041114
152474616824746169AG23GENIChomozygous48479713
152474627324746274TG22GENIChomozygous48479715
152474778924747790TC22GENIChomozygous48479717
152474779824747799CG24GENIChomozygous48479719
152474797824747979CCT4GENIChomozygous48479721
152474803524748036T-3GENIChomozygous48479723
152474862924748630GC34GENIChomozygous48479725
152474890624748907GA32GENIChomozygous48479727
152474903524749036TTGAGAGAGA11GENICheterozygous49425961
152474980024749801GA37GENIChomozygous48479729
152474809324748094T-1GENIChomozygous49220500
152474813024748131C-3GENICheterozygous49359010
152474903524749036TTGAGAGA11GENICpossibly homozygous49359012
152474903724749038TA14GENIChomozygous49359013
152474903924749040TA14GENIChomozygous49359014