chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95269061252690613TC19GENIChomozygous117339414
95269138452691385GT28GENIChomozygous117339415
95269182952691830TC26GENIChomozygous117339416
95269416152694162TC23GENIChomozygous117339417
95269417252694173GT23GENIChomozygous117339418
95269425752694258GA35GENIChomozygous117339419
95269517452695175AG15GENIChomozygous117339420
95269676252696763GA21GENIChomozygous117339421
95269676552696766AG22GENIChomozygous117339422
95269767352697674AG27GENIChomozygous117339423
95269902952699030TC13GENIChomozygous117339424
95270136152701362AC29GENIChomozygous117339425
95270173652701737AG19GENIChomozygous117339426
95270230652702307GA26GENIChomozygous117339427
95270302152703022CT26GENIChomozygous117339428
95270404652704047CT35GENIChomozygous117339430
95270700652707007GC22GENIChomozygous117339431
95270763852707639CT18GENIChomozygous117339432
95270845852708459TG24GENIChomozygous117339433
95270865452708655AG26GENIChomozygous117339434
95270954552709546GA30GENIChomozygous117339435
95271042352710424TA28GENIChomozygous117339436
95271166652711667GA22GENIChomozygous117339437
95271167752711678GA23GENIChomozygous117339438
95271369252713693GA21GENIChomozygous117339439
95271562752715628TC29GENIChomozygous117545714
95271562952715630AT29GENIChomozygous117545716
95271602552716026CA29GENIChomozygous117339440
95271609252716093AT36GENIChomozygous117339441