chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123516888123516889AG3GENIChomozygous54090238
7123516890123516891AAG1GENIChomozygous54090239
7123517388123517389CCAACA3GENIChomozygous54090244
7123518850123518851TA5GENIChomozygous54090245
7123520676123520677AT3GENICheterozygous54090247
7123520731123520732TA12GENIChomozygous54090248
7123521354123521355CT8GENIChomozygous54090250
7123521573123521574GC10GENIChomozygous54090251
7123522131123522132AG12GENIChomozygous54090253
7123522481123522482CT2GENIChomozygous54090256
7123522732123522733CCA2GENICheterozygous54090257
7123523040123523041AG12GENICheterozygous54090259
7123523513123523514TG11GENIChomozygous54090260
7123524801123524802CT13GENICpossibly homozygous54090263
7123524911123524912GGTTT4GENICheterozygous54236479
7123529167123529168CCGTGT2GENIChomozygous54236501