chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
996903579690358CA42GENIChomozygous117243413
996908399690840TC30GENIChomozygous117243414
996909439690944AT6GENICheterozygous117482433
996912549691255AG49GENIChomozygous117243415
996918299691830GA47GENICpossibly homozygous117243416
996920299692030AC64GENIChomozygous117243417
996923739692374TC57GENIChomozygous117243418
996925509692551GA54GENIChomozygous117243419
996925939692594AG60GENIChomozygous117243420
996927529692753TG68GENIChomozygous117243421
996928399692840TA56GENIChomozygous117243422
996931079693108CT55GENIChomozygous117243423
996936339693634CA29GENICpossibly homozygous117243425
996937209693721TC43GENIChomozygous117243426
996938959693896CT59GENICpossibly homozygous117243427
996939189693919CA69GENICpossibly homozygous117243428
996944329694433TA47GENICpossibly homozygous117243429
996946459694646AG67GENIChomozygous117243430
996952679695268CA33GENIChomozygous117243431
996953159695316TC42GENIChomozygous117243432
996954729695473TC53GENIChomozygous117243433
996960689696069AG169GENICheterozygous117243434
996960699696070AG174GENICheterozygous117243435
996972359697236CT72GENIChomozygous117243437
996975369697537CT65GENICpossibly homozygous117243438
996982469698247AG50GENIChomozygous117243439
996983249698325AG51GENIChomozygous117243440
996984819698482TC43GENIChomozygous117243441
996997879699788AG63GENIChomozygous117243442
996998419699842GA64GENIChomozygous117243443
997002599700260TA32GENICpossibly homozygous117482435
997002639700264TA35GENICpossibly homozygous117243444
997020559702056CT63GENIChomozygous117243445
997022649702265CT36GENIChomozygous117243446