chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69338651893386519AC13GENIChomozygous115072229
69339166993391670CA28GENIChomozygous114903339
69339341793393418CT10GENIChomozygous114903341
69339356593393566AT14GENIChomozygous114903343
69339501293395013CT29GENIChomozygous114903345
69339609393396094CT24GENIChomozygous114903347
69339652793396528TC25GENIChomozygous114903349
69339765793397658TC30GENIChomozygous114903352
69339794093397941AG23GENIChomozygous114903354
69340072193400722CT33GENIChomozygous114903356
69340170393401704GT38GENIChomozygous114903358
69340213493402135AG35GENIChomozygous114903360
69340229493402295CT37GENIChomozygous114903362
69340289993402900AG11GENIChomozygous114903364
69340346693403467CT32GENIChomozygous114903366
69340358793403588CA21GENIChomozygous114903368
69340447893404479TC13GENIChomozygous114903370
69340489093404891CA18GENIChomozygous114903372
69340510393405104TC29GENIChomozygous114903374
69340524393405244CT25GENIChomozygous114903376
69340639193406392CT14GENIChomozygous114903378
69340676793406768AG43GENIChomozygous114903380
69340677293406773GA41GENIChomozygous115139373
69340680093406801GC36GENIChomozygous114903382
69340737693407377AT25GENIChomozygous114903384
69340786193407862GA16GENIChomozygous114903386
69340816493408165CT24GENIChomozygous114903388
69340821093408211GT29GENIChomozygous114903390
69340899193408992GC28GENIChomozygous114903392
69341058293410583CA14GENIChomozygous114903394
69341135893411359CT28GENIChomozygous114903396
69341136193411362CT26GENIChomozygous114903398