chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106781223567812236GT29GENIChomozygous116796529
106781275267812753AC37GENIChomozygous116796531
106781432167814322TG19GENIChomozygous116796533
106781517767815178AG12GENIChomozygous116796535
106781614867816149AG24GENIChomozygous116796537
106781636167816362CT32GENIChomozygous116796539
106781644467816445TC33GENIChomozygous116796541
106782415467824155AT26GENIChomozygous116796543
106782933367829334AC13GENICheterozygous117220817
106782995067829951CT27GENIChomozygous116796545
106783129467831295GA23GENIChomozygous116796547
106783418367834184AG21GENIChomozygous116796549
106783461767834618TC18GENIChomozygous116796551
106783566867835669CT18GENIChomozygous116796553
106783983867839839CA22GENIChomozygous116796555
106783989967839900TC17GENIChomozygous116796557
106784219567842196CT20GENIChomozygous116796559
106784266967842670CT15GENIChomozygous116796561
106784369367843694CT6GENIChomozygous117179729
106784851967848520GA33GENIChomozygous116796563
106785240367852404CT27GENIChomozygous116796565
106785251267852513GT23GENIChomozygous116796567
106785686367856864AG16GENIChomozygous116796569
106785298867852989GA25GENICpossibly homozygous118068268
106782500867825009AG15GENIChomozygous116942639
106784343467843435AG27GENIChomozygous116942641
106784365267843653CT12GENIChomozygous117196382