chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274616718274616719GA24GENICpossibly homozygous108655233
1274616794274616795CT21GENIChomozygous108655235
1274618088274618089CT26GENIChomozygous108655239
1274618249274618250AC28GENIChomozygous108655241
1274618901274618902TC18GENIChomozygous108655243
1274618905274618906TC18GENIChomozygous108655245
1274619202274619203CT42GENICheterozygous108655247
1274619254274619255CT45GENICheterozygous108655249
1274619281274619282AG34GENICheterozygous108655251
1274619308274619309GT16GENICpossibly homozygous108655253
1274619336274619337CG22GENICheterozygous108655255
1274619418274619419CT28GENICheterozygous108655257
1274619438274619439CG31GENICheterozygous108655260
1274619564274619565GC27GENICheterozygous108655262
1274619570274619571CG28GENICheterozygous108655264
1274619663274619664GA23GENICpossibly homozygous108655266
1274620081274620082AG21GENIChomozygous108655268
1274620217274620218GA25GENIChomozygous108655270
1274620235274620236CT22GENIChomozygous108655271
1274620980274620981GA25GENIChomozygous108655273
1274621733274621734AC19GENIChomozygous108655275
1274621818274621819GA22GENIChomozygous108655277
1274641490274641491TC25GENIChomozygous108655279
1274641942274641943TC28GENIChomozygous108655281