chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3134684987134684990TTT---1GENIChomozygous57689004
3134684990134684991TA1GENIChomozygous58624925
3134685303134685304AG58GENIChomozygous57689006
3134685844134685845TA30GENIChomozygous58201565
3134685984134685985TA28GENIChomozygous58201567
3134686227134686228CT27GENIChomozygous57689008
3134686230134686231AG27GENIChomozygous57689009
3134686614134686615CT36GENIChomozygous57689011
3134688007134688008T-29GENIChomozygous58395366
3134685516134685517GC31GENIChomozygous58395363
3134685886134685887CT37GENIChomozygous58395364
3134686043134686044AG37GENIChomozygous58395365
3134688397134688398CT26GENIChomozygous58395367
3134688914134688915GA29GENIChomozygous58395368
3134688980134688981AG18GENIChomozygous58395369
3134689049134689050CT11GENIChomozygous58395370
3134689145134689146TTTTTG15GENIChomozygous57689016
3134689180134689181AG18GENIChomozygous58395371
3134689185134689186T-19GENIChomozygous58395372
3134689231134689232AAG13GENIChomozygous58395373
3134689240134689241TG14GENIChomozygous58561284
3134689241134689242TG15GENIChomozygous58561285
3134689245134689246TG14GENIChomozygous58395374
3134689267134689268GA15GENIChomozygous58395375
3134689369134689370AT18GENIChomozygous58395376
3134689534134689535CA32GENIChomozygous58395377
3134689785134689786GC26GENIChomozygous58395378
3134689853134689854AG27GENIChomozygous58395379
3134690775134690776AT19GENIChomozygous58395380
3134691341134691342AG15GENIChomozygous58395381
3134691912134691916ACAT----17GENIChomozygous58395382
3134691951134691953AG--27GENIChomozygous58395383
3134692138134692139GT20GENIChomozygous58395384
3134692319134692320CA28GENIChomozygous58395385
3134692735134692736TC27GENIChomozygous57689019
3134693996134693997TTA15GENIChomozygous58395386
3134694408134694409GA39GENIChomozygous58696352
3134694441134694442GA40GENIChomozygous58395387