chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1247507389247507390AC55GENIChomozygous108602896
1247507426247507427TA65GENIChomozygous108602897
1247507485247507486TG53GENIChomozygous120907097
1247510104247510105CG60GENIChomozygous108602899
1247511571247511572AG68GENIChomozygous108602903
1247511580247511581CT66GENIChomozygous120878792
1247511981247511982CT62GENIChomozygous120878793
1247512289247512290TC72GENIChomozygous108602904
1247512314247512314T66GENIChomozygous127501467
1247512478247512479GA65GENIChomozygous120903015
1247513265247513265TTCCCTCCGTCCCTTGACCTGTTCTA30GENIChomozygous131265587
1247514372247514373GA89GENIChomozygous109017660
1247514378247514379GA89GENIChomozygous108602907
1247514380247514381CT90GENIChomozygous120903016
1247514514247514515TC68GENIChomozygous120903017