chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274616718274616719GA27GENIChomozygous108655233
1274616794274616795CT28GENIChomozygous108655235
1274618088274618089CT27GENIChomozygous108655239
1274618249274618250AC21GENIChomozygous108655241
1274619308274619309GT9GENIChomozygous108655253
1274619418274619419CT17GENIChomozygous108655257
1274619319274619321AT12GENIChomozygous132795977
1274619323274619327ACAG13GENIChomozygous132795978
1274619439274619439ACACAGACACACAG20GENIChomozygous127513008
1274619564274619565GC18GENIChomozygous108655262
1274619570274619571CG15GENIChomozygous108655264
1274619663274619664GA32GENIChomozygous108655266
1274620081274620082AG35GENIChomozygous108655268
1274620217274620218GA32GENIChomozygous108655270
1274620235274620236CT30GENIChomozygous108655271
1274620550274620551T30GENIChomozygous127513009
1274620980274620981GA30GENIChomozygous108655273
1274621008274621014GGCCTC34GENIChomozygous127513010
1274621733274621734AC32GENIChomozygous108655275
1274621818274621819GA36GENIChomozygous108655277
1274641490274641491TC25GENIChomozygous108655279
1274641942274641943TC20GENIChomozygous108655281