chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134803210948032110AC33GENIChomozygous114548661
134803274848032749CT27GENIChomozygous114669176
134803326848033269AG30GENICheterozygous118497742
134803668748036688TC25GENIChomozygous114548665
134803676248036763GA25GENIChomozygous114615403
134803714548037146GC24GENIChomozygous114615404
134803745348037454CT38GENIChomozygous114615405
134803763148037632GT29GENIChomozygous114615406
134803781448037815TG26GENIChomozygous114548668
134803793848037939AG21GENIChomozygous114548670
134803827848038279AG23GENIChomozygous114548671
134803885248038853CT17GENIChomozygous114548672
134803968848039689AG35GENIChomozygous114548674
134803971548039716TC33GENIChomozygous114548675
134804046448040465AT26GENIChomozygous114669178
134804194748041948TC12GENICpossibly homozygous118521616
134804436848044369TC22GENIChomozygous114615413
134804441448044415CT27GENIChomozygous114548680
134804473648044737AG30GENIChomozygous114548681
134804553448045535CT39GENIChomozygous114548682
134804617448046175AC29GENIChomozygous114548683
134804640948046410AT26GENIChomozygous114548684
134804730648047307AG34GENIChomozygous114548685
134804855548048556AG30GENIChomozygous114548686
134804978148049782GA23GENIChomozygous114548687
134805096148050962AG25GENIChomozygous114548688
134805209048052091AC34GENIChomozygous114548689
134805332948053330TC29GENIChomozygous114548690
134805543348055434AG36GENIChomozygous114548695
134804191948041920CT14GENICheterozygous118535354