chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3134685303134685304AG19GENICpossibly homozygous57689006
3134685516134685517GC11GENIChomozygous58395363
3134685844134685845TA6GENICheterozygous58201565
3134685886134685887CT12GENICpossibly homozygous58395364
3134685984134685985TA15GENIChomozygous58201567
3134686043134686044AG19GENIChomozygous58395365
3134686227134686228CT11GENICheterozygous57689008
3134686230134686231AG11GENICpossibly homozygous57689009
3134686614134686615CT26GENIChomozygous57689011
3134686905134686906T-1GENIChomozygous57689012
3134688007134688008T-13GENIChomozygous58395366
3134688397134688398CT17GENIChomozygous58395367
3134688914134688915GA5GENIChomozygous58395368
3134688980134688981AG4GENIChomozygous58395369
3134689049134689050CT11GENICpossibly homozygous58395370
3134689180134689181AG5GENIChomozygous58395371
3134689185134689186T-5GENIChomozygous58395372
3134689231134689232AAG4GENIChomozygous58395373
3134689245134689246TG3GENIChomozygous58395374
3134689267134689268GA10GENIChomozygous58395375
3134689369134689370AT11GENIChomozygous58395376
3134689534134689535CA8GENIChomozygous58395377
3134689785134689786GC10GENIChomozygous58395378
3134689853134689854AG18GENIChomozygous58395379
3134690775134690776AT17GENIChomozygous58395380
3134691341134691342AG20GENIChomozygous58395381
3134691951134691953AG--5GENIChomozygous58395383
3134692319134692320CA6GENICheterozygous58395385
3134693996134693997TTA2GENIChomozygous58395386
3134694441134694442GA13GENIChomozygous58395387
3134689241134689242TG2GENIChomozygous58561285