chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
16024874460248745GC30GENICheterozygous108117826
16024878060248781AT30GENICheterozygous108117828
16024889260248893TC29GENICheterozygous109414035
16024889860248899CA27GENICheterozygous108117829
16024894860248949GC27GENICheterozygous108117830
16024895060248951TA27GENICheterozygous108117831
16024895160248952GC27GENICheterozygous108117832
16024899160248992TA37GENICheterozygous108117833
16024905160249052GA37GENICheterozygous108117834
16024911560249116TA32GENICheterozygous108117835
16024929460249295TA23GENICheterozygous108117836
16024929760249298TC20GENICheterozygous108117837
16024933060249331CT35GENICheterozygous108117838
16024953860249539AG43GENICheterozygous108117839
16024953960249540AG43GENICheterozygous108117840
16024962460249625CG19GENICheterozygous108117841
16024917760249178TA35GENICheterozygous109486469