chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4104365918104365919TC49GENIChomozygous137186303
4104365999104366000TG38GENIChomozygous137186304
4104366222104366223TG41GENICpossibly homozygous137186305
4104366503104366503TG44GENIChomozygous136909075
4104367533104367534TC55GENIChomozygous137186306
4104367948104367949GT54GENIChomozygous137186307
4104368237104368238CT51GENIChomozygous137186308
4104368328104368329AG43GENIChomozygous137186309