chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1220691062069107TG12GENIChomozygous115512562
1220694572069458GA23GENIChomozygous115512563
1220695252069526GA23GENIChomozygous115512564
1220711472071148GA12GENIChomozygous115512565
1220717002071701GA11GENIChomozygous115233564
1220719002071901TC21GENIChomozygous115233566
1220721172072118TC11GENIChomozygous115233568
1220732462073247CT23GENIChomozygous115512566
1220737392073740TC22GENIChomozygous115233576
1220737972073798TC18GENIChomozygous115233578
1220752252075225GGTTATTCAACTCGACCTTTGAA22GENIChomozygous128949003
1220705382070539AG12GENIChomozygous115357225
1220715812071583GT17GENICpossibly homozygous134301059
1220733952073427CACACAGACACACCTACATACACAGACACACT12GENIChomozygous134301060
1220752582075258T19GENIChomozygous128949004
1220755182075521AGT19GENIChomozygous134301061
1220756282075629CT19GENIChomozygous115512567
1220757042075705AG19GENIChomozygous115512568
1220767622076763CT16GENIChomozygous115512569
1220779632077963T14GENIChomozygous128949005
1220821152082116GA19GENIChomozygous115512570
1220832422083242AC19GENIChomozygous134301062
1220834172083454GCACACAGCACACATACACACACACGCACACATACAC7GENIChomozygous134301063
1220843862084387CG14GENIChomozygous115512571
1220971182097119GA14GENIChomozygous115512572
1220981102098111CT13GENIChomozygous115512573
1220752642075265GA19GENIChomozygous115490609
1220948112094812GA8GENIChomozygous134302037