chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34060146140601462CT33GENICheterozygous784534343
34060147840601479CT33GENICheterozygous784534344
34060149640601497GT35GENICheterozygous784534345
34060150240601503GA34GENICheterozygous784534346
34060150540601506CT35GENICheterozygous784534347
34060160540601606GT29GENICheterozygous784534348
34060160740601608TA29GENICheterozygous784534349
34060162140601622TC34GENICheterozygous784534350
34060162440601625GA33GENICheterozygous784534351
34060167340601674AG39GENICheterozygous784534352
34060185240601853CT35GENICheterozygous784534353
34060185340601854CG35GENICheterozygous784534354
34060190740601908TC39GENICheterozygous784534355
34060192540601926TC44GENICheterozygous784534356
34060194640601947GA41GENICheterozygous784534357
34060194840601949GA41GENICheterozygous784534358
34060196140601962TC45GENICheterozygous784534359
34060197240601973CT46GENICheterozygous784534360
34060197740601978AG46GENICheterozygous784534361
34060198240601983GA43GENICheterozygous784534362
34060199340601994TC39GENICheterozygous784534363
34060199440601995GA40GENICheterozygous784534364