chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264226142264226143CG21GENIChomozygous610053685
1264226915264226916TA20GENIChomozygous610053686
1264228792264228793AG26GENIChomozygous610053687
1264229042264229043GGT6GENIChomozygous734002492
1264229240264229241CCGT14GENICheterozygous734002493
1264229240264229241CCGTGT14GENICheterozygous734002494
1264229310264229311TC19GENIChomozygous610053688
1264230653264230654GGTTT8GENIChomozygous734002498
1264230657264230658GT12GENIChomozygous610053689
1264231202264231203GGTGGTT15GENIChomozygous734002499
1264231476264231477A-10GENIChomozygous734002500
1264231777264231813AAGAAAGGAAGAAAGGAAGAAAGAAAGAAAGAAAGA------------------------------------9GENIChomozygous734002501
1264232052264232053TC12GENIChomozygous610053690
1264233092264233093GA13GENIChomozygous610053691
1264235077264235078GA25GENIChomozygous610053692
1264235389264235390G-16GENIChomozygous734002503
1264235499264235501TT--8GENIChomozygous734002504
1264235937264235938T-7GENIChomozygous734002508
1264236612264236613AG27GENICpossibly homozygous610053693
1264237110264237111CG35GENIChomozygous612341192
1264237128264237129GT27GENIChomozygous610053694
1264237824264237825GC31GENIChomozygous610053695
1264237845264237846GA21GENIChomozygous610053696
1264237893264237894CT21GENIChomozygous610053697
1264237932264237933CA23GENIChomozygous610053698
1264238519264238520TC26GENIChomozygous610053699
1264239237264239238AG21GENIChomozygous610053700
1264239837264239838GA18GENIChomozygous610053701
1264240127264240130TTT---5GENIChomozygous734002509
1264240267264240268AG19GENIChomozygous612341193
1264240881264240882AG23GENIChomozygous610053702
1264240961264240962AG28GENIChomozygous610053703
1264241000264241001AG32GENIChomozygous610053704
1264241159264241160GA14GENIChomozygous610053705