chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106047441160474458ACACACACACACACACACACACACACACACACAGCTTGGCCTGGTGT9GENICheterozygous138686263
106047586660475867AG25GENIChomozygous138801315
106047784660477847CA29GENIChomozygous138801317
106048217060482171GA28GENIChomozygous138801318
106048428060484282TG18GENICpossibly homozygous138686264
106048764660487647CT8GENIChomozygous138801319
106048833260488333GC21GENIChomozygous138801320
106048936960489369TTTGT16GENIChomozygous138686265
106049411460494118CTTC17GENIChomozygous138686266