chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117744886177448862AG62GENIChomozygous50893275
117744954877449549TC70GENIChomozygous50893277
117745096077450961AG57GENIChomozygous50893279
117745107377451074TA72GENIChomozygous50893281
117745117077451171GA54GENIChomozygous50893283
117745157777451578AC54GENIChomozygous50893285
117745183477451835TC70GENIChomozygous50893287
117745240977452410TTA51GENIChomozygous50893289
117745243177452432GT46GENIChomozygous50893291
117745296277452963T-69GENIChomozygous50893293
117745315677453157CT58GENIChomozygous50893295
117745320777453208A-1GENIChomozygous50893297
117745330977453310GC51GENIChomozygous50893299
117745390077453903AAA---28GENIChomozygous50893301
117745396477453965TTAGCA20GENIChomozygous50893303
117745396877453969T-18GENIChomozygous50893305
117745520577455206AG76GENIChomozygous50893307
117745544977455450GA56GENICpossibly homozygous50893309
117745549577455496CCTCT33GENIChomozygous50893311
117745553477455535T-39GENIChomozygous50893313
117745585877455859AG45GENIChomozygous50893315
117745585977455860AC45GENIChomozygous50893317
117745634677456347AG75GENIChomozygous50893319
117745654177456542GA47GENIChomozygous50893321
117745655277456553GA42GENIChomozygous50893323
117745670177456702CA46GENIChomozygous50893325
117745690277456903TC33GENICpossibly homozygous50893327
117745692177456926ATTTT-----28GENIChomozygous50893328
117745703577457036GA59GENIChomozygous50893330
117745703777457038A-57GENIChomozygous50893332
117745705277457053GA44GENIChomozygous50893334
117745708277457083TC49GENIChomozygous50893336
117745711977457120TA48GENIChomozygous50893338
117745712177457122CT48GENIChomozygous50893340
117745716277457163TA53GENIChomozygous50893342
117745728877457289TC59GENIChomozygous50893343
117745733277457333AG60GENIChomozygous50893345