chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125743344125743345AT25GENIChomozygous663927501
7125743354125743355CA27GENIChomozygous663927502
7125744815125744816GA31GENIChomozygous663927503
7125745572125745580TGTGTGTA--------8GENIChomozygous765449844
7125747094125747095CT35GENIChomozygous663927504
7125747095125747096CT35GENIChomozygous663927505
7125747420125747421GA28GENIChomozygous663927506
7125747534125747535CT32GENICpossibly homozygous663927507
7125747647125747655CAACATGA--------26GENIChomozygous765449845
7125747681125747682TG31GENIChomozygous663927508
7125747731125747733TG--33GENIChomozygous765449846
7125748235125748236TC26GENIChomozygous663927509
7125748533125748534TC39GENIChomozygous663927510
7125748640125748641CG20GENIChomozygous663927511
7125748927125748928GA32GENIChomozygous663927512
7125749414125749415AG20GENIChomozygous663927513
7125749577125749578GGGCAGTCAGTGCCC17GENIChomozygous765449847
7125749657125749658GT23GENIChomozygous663927514
7125751261125751262GA26GENIChomozygous663927515
7125751521125751522AAT12GENICheterozygous765449848
7125752000125752001TC22GENIChomozygous663927516
7125753821125753822CT21GENIChomozygous663927517
7125753897125753898CT30GENIChomozygous663927518
7125753949125753950GA28GENIChomozygous663927519
7125754274125754275AG25GENIChomozygous663927520
7125754320125754321CT26GENIChomozygous663927521
7125754367125754368CT32GENIChomozygous663927522
7125754379125754380GC32GENIChomozygous663927523
7125755157125755158GA21GENIChomozygous663927524
7125755666125755667CT39GENIChomozygous663927525
7125755703125755704CT33GENIChomozygous663927526
7125756500125756501TC32GENIChomozygous663927527
7125756849125756850AG19GENIChomozygous663927528
7125756965125756966GGAAAA6GENICheterozygous765449851
7125756965125756966GGAAAAAAAAAAA6GENICheterozygous765449852
7125757153125757154TTA14GENIChomozygous765449853