chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5126166284126166285AC21GENIChomozygous113996572
5126166507126166508AC19GENIChomozygous113996576
5126166941126166942TC12GENIChomozygous113996579
5126168430126168431GA16GENIChomozygous114137108
5126171274126171275CT25GENIChomozygous113996595
5126171453126171454TC24GENIChomozygous113996597
5126172079126172080GA20GENIChomozygous114137109
5126172934126172935TC5GENIChomozygous113996607
5126173208126173209AG11GENIChomozygous113996609
5126173476126173477TC12GENIChomozygous113996613
5126174024126174025AG11GENIChomozygous113996615
5126175600126175601CT12GENIChomozygous113996617
5126175784126175785AG26GENIChomozygous113996618
5126175867126175868CT10GENIChomozygous113996620
5126175903126175904AG17GENIChomozygous113996622
5126178445126178446AG22GENIChomozygous113996624
5126179112126179113AG9GENIChomozygous113996626
5126179863126179864CG16GENIChomozygous113996628
5126182103126182104AG9GENIChomozygous113996630
5126182139126182140GT4GENIChomozygous126260256
5126186983126186984AC15GENIChomozygous113996632
5126187664126187665AG13GENIChomozygous113996634
5126188582126188583GA13GENIChomozygous113996636
5126182138126182139AG4GENIChomozygous126202892