chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117734094117734095GA26GENIChomozygous113153244
4117734526117734527TC25GENIChomozygous112820028
4117734709117734710TC26GENIChomozygous112820030
4117734710117734711GA27GENIChomozygous113153245
4117734969117734970TC23GENIChomozygous113153246
4117735595117735596CT16GENIChomozygous113153247
4117735673117735674CT26GENIChomozygous112820032
4117735876117735877CT27GENIChomozygous113153248
4117736697117736698CA25GENIChomozygous113153249
4117736857117736858CT21GENIChomozygous113153250
4117736940117736941TC21GENIChomozygous113153251
4117737260117737261CT29GENIChomozygous112820034
4117737765117737766CT22GENIChomozygous113153252
4117737883117737884GA26GENIChomozygous113153253
4117738587117738588TG26GENIChomozygous112820036
4117738820117738821AG15GENICpossibly homozygous113153254
4117739693117739694GA19GENIChomozygous113153255
4117739991117739992GA18GENICheterozygous113153256
4117740746117740747AG22GENIChomozygous113153257
4117741295117741296AG30GENIChomozygous112820038
4117741400117741401GA29GENIChomozygous112820040
4117742578117742579TC20GENIChomozygous112820042
4117742999117743000AG27GENIChomozygous112820044
4117743276117743277TC28GENIChomozygous113153258
4117743714117743715TC22GENIChomozygous113153259
4117744154117744155AG14GENIChomozygous113153260
4117744365117744366CT9GENIChomozygous113153261
4117744619117744620GA19GENICpossibly homozygous113153262
4117744736117744737CT20GENIChomozygous113153263
4117744879117744880AG24GENIChomozygous113153264
4117745283117745284GC20GENIChomozygous113153265
4117745398117745399TC19GENIChomozygous113153266
4117745471117745472AG22GENIChomozygous113153267
4117745484117745485TA19GENIChomozygous113153268