chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264094064264094065AG18GENIChomozygous885238209
1264094170264094171GT18GENIChomozygous885238210
1264094246264094247TC15GENIChomozygous885238211
1264094261264094262TC18GENIChomozygous885238212
1264095002264095003TC18GENIChomozygous885238213
1264095870264095871CT14GENIChomozygous885238214
1264095886264095887AG7GENIChomozygous885238215
1264096067264096068CG9GENIChomozygous885238216
1264096649264096650CT27GENIChomozygous885238217
1264096802264096803GA18GENIChomozygous885238218
1264096893264096894CA11GENIChomozygous885238219
1264096989264096990AG18GENIChomozygous885238220
1264097432264097433TC17GENIChomozygous885238221
1264097484264097485TC26GENIChomozygous885238222
1264097567264097568GA10GENIChomozygous885238223
1264097573264097574GC10GENIChomozygous885238224
1264097633264097634AC19GENIChomozygous885238225
1264097768264097769AG21GENIChomozygous885238226
1264097829264097830TC25GENIChomozygous885238227
1264097921264097922AC10GENIChomozygous885238228
1264097923264097924AT9GENIChomozygous885238229
1264098005264098006CA8GENIChomozygous885238230
1264098124264098125TC17GENIChomozygous885238231
1264098178264098179GA16GENIChomozygous885238232
1264099341264099342AG6GENIChomozygous885238233
1264099366264099367GA13GENIChomozygous885238234
1264099541264099542GA20GENIChomozygous885238235
1264100050264100051GC15GENIChomozygous885238236
1264100637264100638TC17GENIChomozygous885238237
1264100900264100901TG10GENICheterozygous885238238
1264102249264102250GA14GENICheterozygous885238239
1264102726264102727TA4GENICheterozygous885238240
1264102803264102804CT17GENIChomozygous885238241
1264103344264103345CT23GENIChomozygous885238242
1264103826264103827GT19GENIChomozygous885238243
1264104691264104692CT14GENIChomozygous885238244