chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141434565141434566GT50GENIChomozygous108260665
1141434568141434568A52GENIChomozygous127438911
1141436965141436966CT72GENIChomozygous108260667
1141439701141439703AC51GENIChomozygous127438912
1141439704141439710GCACAG51GENIChomozygous127438913
1141440402141440407ATAAC31GENIChomozygous127438914
1141451814141451838CTTGGGCTGGTCCCACCTTCCCCA38GENIChomozygous127438915
1141451983141451984GT47GENICpossibly homozygous108260671
1141439710141439711CT51GENIChomozygous120473769