chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266844654266844654GGCGGC11GENIChomozygous127509292
1266845636266845637CT13GENIChomozygous108638680
1266845640266845641GA13GENIChomozygous108638681
1266846660266846661CT22GENIChomozygous108638682
1266847220266847221CA23GENIChomozygous108638683
1266847278266847279GA19GENIChomozygous108638684
1266847339266847340CA20GENIChomozygous108638685
1266847359266847360CA22GENIChomozygous108638686
1266848538266848539TC21GENIChomozygous108638687
1266849700266849701TC26GENIChomozygous108638688
1266849901266849902CG22GENIChomozygous108638689
1266850266266850267GA20GENIChomozygous108638690
1266850741266850742AG23GENIChomozygous108638691
1266851391266851392CT25GENIChomozygous108638692
1266851543266851544AC27GENIChomozygous108638693
1266851785266851786GA10GENIChomozygous108638694
1266848660266848661T23GENIChomozygous127509293
1266850951266850962GGGAGAAGCAG27GENIChomozygous127509294
1266851942266851943AG16GENIChomozygous108638695
1266854156266854157AC6GENIChomozygous108638696
1266854407266854408TC7GENIChomozygous108638697
1266854684266854684TG19GENIChomozygous127509295
1266855702266855703TC27GENIChomozygous108638698
1266855772266855773TC20GENIChomozygous108638699
1266856268266856269CG14GENIChomozygous108638700
1266856629266856629TGTTATAA16GENIChomozygous127509296
1266858119266858120AG19GENIChomozygous108638701
1266858271266858272CT19GENIChomozygous108638702
1266858612266858612AT20GENIChomozygous127509297
1266858867266858868AG12GENIChomozygous108638703
1266858919266858920TC11GENIChomozygous108638704
1266859443266859444A23GENIChomozygous127509298
1266859629266859630CT18GENIChomozygous108638705
1266859655266859656TC18GENIChomozygous108638706