chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6146124492146124493CCGTGTGT22GENICheterozygous695760329
6146124492146124493CCGTGTGTGT22GENICpossibly homozygous695760330
6146125686146125687TG35GENICheterozygous537000279
6146125754146125757AAA---4GENIChomozygous695760331
6146126397146126398CT32GENIChomozygous537000280
6146127571146127572CT29GENIChomozygous534144158
6146127830146127840GCGTGTGTGA----------24GENICpossibly homozygous695760332
6146127841146127842CA32GENICheterozygous534144159
6146127868146127874GTGTGT------16GENICheterozygous695760333
6146128730146128731CA55GENIChomozygous537000281
6146130058146130059AG55GENIChomozygous534144160
6146130280146130281CT52GENIChomozygous534144161