chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4116869442116869443CA37GENIChomozygous113152375
4116869457116869458GA42GENIChomozygous113152376
4116869754116869755GA31GENIChomozygous113152377
4116870454116870455AG23GENIChomozygous113152378
4116870575116870576TC32GENIChomozygous113152379
4116870682116870683TG29GENIChomozygous113152380
4116870868116870869CT25GENIChomozygous113152381
4116871051116871052TA35GENIChomozygous113152382
4116871707116871708CT25GENIChomozygous113152383
4116872164116872165GC27GENIChomozygous113152384
4116872200116872201CT37GENIChomozygous113152385
4116872229116872230TG37GENIChomozygous113152386
4116872695116872696GA17GENIChomozygous113152387
4116872815116872816TC21GENIChomozygous113152388
4116873019116873020GA26GENIChomozygous113152389
4116873335116873336CG32GENIChomozygous113152390
4116873563116873564GA17GENIChomozygous113152391
4116873854116873855AG19GENIChomozygous113152392
4116873964116873965TC22GENIChomozygous113152393
4116874138116874139CT25GENIChomozygous113152394
4116874427116874428GA29GENIChomozygous113152395
4116874829116874830CT26GENIChomozygous113152396
4116875090116875091AG28GENIChomozygous113152397
4116875400116875401TC41GENIChomozygous113152398
4116875448116875449CT44GENIChomozygous113152399
4116875546116875547TC28GENIChomozygous113152400
4116875564116875565CT30GENIChomozygous113152401
4116875623116875624GA36GENIChomozygous113152402
4116876005116876006TC28GENIChomozygous113152403
4116876087116876088GA37GENIChomozygous113152404
4116876145116876146AC22GENIChomozygous113152405
4116876147116876148TC22GENIChomozygous113152406
4116876157116876158AC20GENIChomozygous113152407
4116876160116876161TC18GENIChomozygous113152408