chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3134684987134684990TTT---1GENIChomozygous57689004
3134684990134684991TA1GENIChomozygous58624925
3134685303134685304AG27GENIChomozygous57689006
3134685516134685517GC29GENIChomozygous58395363
3134685844134685845TA14GENIChomozygous58201565
3134685886134685887CT10GENIChomozygous58395364
3134685984134685985TA8GENIChomozygous58201567
3134686043134686044AG18GENIChomozygous58395365
3134686227134686228CT24GENIChomozygous57689008
3134686230134686231AG24GENIChomozygous57689009
3134686614134686615CT34GENIChomozygous57689011
3134686904134686905CCTTT7GENICheterozygous58624926
3134688007134688008T-25GENIChomozygous58395366
3134688397134688398CT18GENIChomozygous58395367
3134688914134688915GA20GENIChomozygous58395368
3134688980134688981AG24GENIChomozygous58395369
3134689049134689050CT19GENIChomozygous58395370
3134689145134689146TTTTTG12GENIChomozygous57689016
3134689180134689181AG17GENIChomozygous58395371
3134689185134689186T-17GENIChomozygous58395372
3134689231134689232AAG15GENIChomozygous58395373
3134689245134689246TG15GENIChomozygous58395374
3134689267134689268GA14GENIChomozygous58395375
3134689369134689370AT15GENIChomozygous58395376
3134689534134689535CA24GENIChomozygous58395377
3134689785134689786GC13GENIChomozygous58395378
3134689853134689854AG16GENIChomozygous58395379
3134690775134690776AT17GENIChomozygous58395380
3134691341134691342AG21GENIChomozygous58395381
3134691912134691916ACAT----14GENIChomozygous58395382
3134691951134691953AG--19GENIChomozygous58395383
3134692138134692139GT16GENIChomozygous58395384
3134692319134692320CA19GENIChomozygous58395385
3134692735134692736TC27GENIChomozygous57689019
3134693996134693997TTA17GENIChomozygous58395386
3134694441134694442GA22GENIChomozygous58395387
3134689240134689241TG15GENIChomozygous58561284
3134689241134689242TG15GENIChomozygous58561285