chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95268913452689135AG37GENICheterozygous117339413
95269061252690613TC47GENIChomozygous117339414
95269138452691385GT42GENIChomozygous117339415
95269182952691830TC23GENIChomozygous117339416
95269416152694162TC46GENIChomozygous117339417
95269417252694173GT55GENIChomozygous117339418
95269425752694258GA48GENIChomozygous117339419
95269517452695175AG43GENIChomozygous117339420
95269676252696763GA39GENIChomozygous117339421
95269676552696766AG40GENIChomozygous117339422
95269767352697674AG32GENIChomozygous117339423
95269902952699030TC42GENIChomozygous117339424
95270136152701362AC19GENIChomozygous117339425
95270173652701737AG30GENIChomozygous117339426
95270230652702307GA35GENIChomozygous117339427
95270302152703022CT38GENIChomozygous117339428
95270341452703415GA21GENIChomozygous117339429
95270404652704047CT22GENIChomozygous117339430
95270700652707007GC28GENIChomozygous117339431
95270763852707639CT37GENIChomozygous117339432
95270845852708459TG59GENIChomozygous117339433
95270865452708655AG49GENIChomozygous117339434
95270954552709546GA13GENIChomozygous117339435
95271042352710424TA25GENIChomozygous117339436
95271166652711667GA23GENIChomozygous117339437
95271167752711678GA26GENIChomozygous117339438
95271369252713693GA38GENIChomozygous117339439
95271602552716026CA26GENIChomozygous117339440
95271609252716093AT26GENIChomozygous117339441