chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274616718274616719GA55GENIChomozygous108655233
1274616794274616795CT70GENIChomozygous108655235
1274618088274618089CT62GENIChomozygous108655239
1274618249274618250AC58GENIChomozygous108655241
1274618931274618931CGAGCAGACACACACACAG9GENIChomozygous132442555
1274619202274619203CT5GENIChomozygous108655247
1274619265274619269ACTT10GENIChomozygous127513006
1274619273274619275AC10GENIChomozygous127513007
1274619297274619298TA12GENIChomozygous121226699
1274619302274619303TC12GENIChomozygous109383698
1274619309274619310AT13GENIChomozygous121226700
1274619314274619315GT12GENIChomozygous121226701
1274619418274619419CT17GENIChomozygous108655257
1274619439274619439ACACAGACACACAG23GENIChomozygous127513008
1274619564274619565GC33GENICpossibly homozygous108655262
1274619570274619571CG31GENICpossibly homozygous108655264
1274619663274619664GA52GENIChomozygous108655266
1274620081274620082AG70GENIChomozygous108655268
1274620217274620218GA59GENIChomozygous108655270
1274620235274620236CT62GENIChomozygous108655271
1274620550274620551T61GENIChomozygous127513009
1274620980274620981GA69GENIChomozygous108655273
1274621008274621014GGCCTC60GENIChomozygous127513010
1274621733274621734AC68GENIChomozygous108655275
1274621818274621819GA85GENIChomozygous108655277
1274641490274641491TC62GENIChomozygous108655279
1274641942274641943TC60GENIChomozygous108655281
1274623399274623399T38GENICheterozygous132266018