chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109664087396640874AG1GENIChomozygous117174018
109664187396641874CT15GENIChomozygous117180444
109664234496642345AG33GENIChomozygous116691712
109664280896642809AG30GENIChomozygous116691714
109664345096643451AC23GENIChomozygous116691718
109664568396645684TC23GENIChomozygous116691720
109664720596647206GC32GENICpossibly homozygous116691722
109664751296647513GC18GENIChomozygous116691724
109664833896648339CT29GENIChomozygous117180445
109665161396651614CT35GENIChomozygous116691738
109665226096652261GT28GENIChomozygous117180446
109665278296652783GC23GENIChomozygous117180447