chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106781223567812236GT14GENIChomozygous961754463
106781275267812753AC20GENIChomozygous961754464
106781432167814322TG19GENIChomozygous961754465
106781517767815178AG23GENIChomozygous961754466
106781636167816362CT22GENIChomozygous961754467
106781644467816445TC17GENIChomozygous961754468
106782415467824155AT21GENIChomozygous961754469
106782500867825009AG14GENIChomozygous961754470
106782995067829951CT26GENIChomozygous961754471
106783129467831295GA11GENIChomozygous961754472
106783418367834184AG10GENIChomozygous961754473
106783461767834618TC10GENIChomozygous961754474
106783983867839839CA24GENIChomozygous961754475
106783989967839900TC25GENIChomozygous961754476
106784219567842196CT25GENIChomozygous961754477
106784266967842670CT13GENIChomozygous961754478
106784343467843435AG32GENIChomozygous961754479
106784851967848520GA28GENIChomozygous961754480
106785251267852513GT24GENICpossibly homozygous961754481
106785686367856864AG16GENIChomozygous961754482