chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
178958477089584771AT25GENIChomozygous930697225
178958490489584905CT22GENIChomozygous930697226
178958566189585662TG12GENIChomozygous930697227
178958648689586487AG41GENIChomozygous930697228
178958676389586764CG51GENIChomozygous930697229
178959383189593832CT26GENIChomozygous930697230
178960077189600772CT22GENIChomozygous930697231
178960109789601098GA30GENIChomozygous930697232
178960116389601164AT34GENIChomozygous930697233
178960444989604450TC41GENIChomozygous930697234
178960506889605069CT27GENIChomozygous930697235
178960560989605610TC20GENIChomozygous930697236
178962055389620554CA30GENIChomozygous930697237
178962141489621415AG27GENIChomozygous930697238
178962240989622410AG41GENIChomozygous930697239
178962251889622519GA35GENIChomozygous930697240
178962621589626216GT33GENIChomozygous930697241
178962790889627909CG29GENIChomozygous930697242
178962994489629945CT14GENIChomozygous930697243
178963061689630617GA24GENIChomozygous930697244
178963371189633712CT24GENIChomozygous930697245
178963562489635625CT40GENICpossibly homozygous930697246
178963806789638068TC31GENIChomozygous930697247
178964042989640430CT39GENIChomozygous930697248
178964805489648055AG55GENIChomozygous930697249
178964915989649160GC16GENIChomozygous930697250
178966028589660286TC56GENIChomozygous930697251
178966126689661267GA11GENIChomozygous930697252
178966160289661603TC9GENIChomozygous930697253
178966253189662532GC40GENIChomozygous930697254
178966448789664488GT19GENIChomozygous930697255
178966452189664522AG21GENIChomozygous930697256
178966489789664898TC49GENIChomozygous930697257
178966563589665636CG20GENIChomozygous930697258