chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106047441160474458ACACACACACACACACACACACACACACACACAGCTTGGCCTGGTGT27GENICheterozygous138686263
106047586660475867AG74GENIChomozygous138801315
106047701360477014GA52GENIChomozygous138801316
106047784660477847CA59GENIChomozygous138801317
106048217060482171GA39GENIChomozygous138801318
106048428060484282TG23GENIChomozygous138686264
106048764660487647CT59GENIChomozygous138801319
106048833260488333GC49GENICpossibly homozygous138801320
106048936960489369TTTGT37GENIChomozygous138686265
106049411460494118CTTC51GENIChomozygous138686266