chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46011835060118351CT56GENICheterozygous113028434
46011841660118417TC57GENICheterozygous112664696
46012415160124152CA22GENICpossibly homozygous112664698
46020367260203673AC22GENICpossibly homozygous112664700
46023059260230593GA23GENIChomozygous112664702
46023453060234531AG18GENICheterozygous112664704
46027058760270588AT66GENICheterozygous112664708
46027063260270633CG49GENICheterozygous112664710
46027834960278350AC3GENIChomozygous112664720
46027835360278354AT3GENIChomozygous112664722
46027835460278355AT3GENIChomozygous112664724
46035269960352700AG29GENIChomozygous112664726
46035318560353186CA22GENICpossibly homozygous112664728