chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1245328698245328699CG18GENICheterozygous810772419
1245328705245328706TG20GENICheterozygous810772420
1245328712245328713AG22GENICheterozygous810772421
1245328759245328760CG30GENICheterozygous810772422
1245328777245328778AT33GENICheterozygous810772423
1245328783245328784GA32GENICheterozygous810772424
1245328824245328825GT28GENICheterozygous810772425
1245328835245328836TC27GENICheterozygous810772426
1245328836245328837GC27GENICheterozygous810772427
1245328841245328842AG27GENICheterozygous810772428
1245328866245328867CT24GENICheterozygous810772429
1245330330245330331GA25GENICheterozygous810772430
1245337915245337916GT23INTERGENIChomozygous810772431
1245337928245337929CT20INTERGENIChomozygous810772432
1245337937245337938CA21INTERGENIChomozygous810772433
1245341810245341811GA31INTERGENICheterozygous810772434
1245341822245341823GA34INTERGENICheterozygous810772435
1245341828245341829CT40INTERGENICheterozygous810772436
1245341833245341834CT44INTERGENICheterozygous810772437
1245341987245341988TC67INTERGENICheterozygous810772438
1245341996245341997AG65INTERGENICheterozygous810772439
1245341997245341998CT61INTERGENICheterozygous810772440
1245342009245342010GA59INTERGENICheterozygous810772441
1245347004245347005TC25INTERGENICheterozygous810772442
1245347008245347009CT28INTERGENICheterozygous810772443
1245347029245347030GA29INTERGENICheterozygous810772444
1245347030245347031GC30INTERGENICheterozygous810772445
1245347060245347061AG34INTERGENICheterozygous810772446
1245347065245347066GC34INTERGENICheterozygous810772447
1245347071245347072AG36INTERGENICheterozygous810772448
1245347074245347075TC30INTERGENICheterozygous810772449
1245347097245347098CT31INTERGENICheterozygous810772450