chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138092949580929496CT29GENIChomozygous114776769
138092993180929932TA33GENIChomozygous114407151
138092993380929934CA32GENIChomozygous114407153
138093331680933317GA35GENIChomozygous114407177
138093355380933554TC30GENIChomozygous114566995
138093687280936873CT20GENIChomozygous114690629
138093946480939465TG17GENIChomozygous114407199
138094049580940496GA34GENIChomozygous114407207
138094950180949502GA24GENIChomozygous114690631
138094967880949679AG23GENIChomozygous114407325
138094975280949753CG27GENIChomozygous114407327
138095000880950009AG21GENIChomozygous114407337
138095149180951492CT28GENIChomozygous114407347
138095151080951511GA25GENIChomozygous114407349
138095153980951540CT23GENIChomozygous114776771
138095188180951882GA26GENIChomozygous114776773
138095190880951909TC28GENIChomozygous114407351
138095300680953007GA24GENIChomozygous114690634
138095332180953322AC28GENIChomozygous114690635
138095354180953542CA30GENIChomozygous114690636
138095404280954043TC31GENIChomozygous114690638
138095515680955157TC32GENIChomozygous114407361
138095531980955320TC27GENIChomozygous114407363
138095537480955375CA38GENIChomozygous114407365
138095571980955720AC45GENIChomozygous114776775
138095575980955760CT28GENIChomozygous114407367
138095626180956262CT36GENIChomozygous114776777
138095635180956352GT27GENIChomozygous114776779
138095642180956422GA33GENIChomozygous114776781
138095725880957259GA42GENIChomozygous114776783
138095752880957529CT38GENIChomozygous114407371
138095822480958225AG30GENIChomozygous114407373
138096334780963348AG28GENIChomozygous114407395
138097166480971665TC27GENIChomozygous114776785
138097474580974746AG24GENIChomozygous114776787
138097715980977160AC34GENIChomozygous114776789
138097854880978549AT24GENIChomozygous114776791
138098597080985971CT31GENIChomozygous114776793