chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185166234251662343TC5GENIChomozygous110347470
185166334551663346GA26GENIChomozygous110347472
185166433951664340CT33GENIChomozygous110347476
185166442051664421CT21GENIChomozygous110473061
185166452851664529TG23GENIChomozygous110347478
185166472251664723TC38GENIChomozygous110347482
185166493451664935CA40GENIChomozygous110473062
185166537651665377AG35GENIChomozygous110347484
185166616751666168GA26GENIChomozygous110347486
185166634051666341CT27GENIChomozygous110347488
185166665151666652GA21GENIChomozygous110347490
185166735351667354GT29GENIChomozygous110347492
185166867551668676CA26GENICpossibly homozygous110703149
185167111351671114GA12GENIChomozygous110473064
185166841851668419GT20GENIChomozygous110347494