chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5152779535152779536AT27GENIChomozygous55929465
5152779590152779591GA31GENIChomozygous55799275
5152779926152779927AG18GENIChomozygous55799277
5152780705152780706TC49GENIChomozygous55929467
5152781066152781067AT25GENIChomozygous55799278
5152782767152782768TA15GENIChomozygous55929469
5152782822152782823AG15GENIChomozygous55799282
5152782979152782980TTC17GENICpossibly homozygous55799283
5152783347152783348TG37GENIChomozygous55929471
5152783352152783353AC34GENIChomozygous55929473
5152784507152784508CT20GENIChomozygous55929479
5152784676152784677GA31GENIChomozygous55929481
5152784858152784859AG27GENIChomozygous55929483
5152784884152784885AC31GENIChomozygous55799294
5152784914152784915GA38GENIChomozygous55929485
5152784918152784919AG38GENIChomozygous55799295
5152785021152785022TG30GENIChomozygous55929487
5152785518152785520TT--25GENIChomozygous55929489
5152785575152785576CT26GENIChomozygous55929491
5152785687152785688AAAAGATCACCAAACAGGG27GENIChomozygous55799296
5152786156152786157CT16GENIChomozygous55799298
5152787238152787239TA16GENIChomozygous55799301
5152787360152787361GA11GENICheterozygous55799302
5152787364152787365GA9GENICheterozygous55799303
5152787373152787374CCA9GENICheterozygous56461261
5152782820152782821GA9GENIChomozygous56461258
5152787331152787332CCAT10GENICheterozygous56461260
5152787394152787395TC14GENIChomozygous55799305