chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4188175714188175715CG10GENICheterozygous826839458
4188178331188178332CCA19GENIChomozygous826839459
4188179922188179923AAAC7GENICheterozygous826839460
4188180500188180501AG8GENICheterozygous826839461
4188187186188187187GGT12GENICheterozygous826839462
4188194677188194678AG19GENICheterozygous826839463
4188195186188195187CA10GENICheterozygous826839464
4188200472188200473GA11GENICheterozygous826839465
4188205452188205453CT10GENICheterozygous826839466
4188205458188205459GA10GENICheterozygous826839467
4188205459188205460GA10GENICheterozygous826839468
4188205490188205492AA--14GENICheterozygous826839469
4188205495188205496GA14GENICheterozygous826839470
4188206584188206585CCA24GENIChomozygous826839471
4188207943188207944GA13GENICheterozygous826839472
4188218451188218452GGA10GENIChomozygous826839473
4188228328188228329CA8GENIChomozygous826839474
4188228335188228336CA10GENIChomozygous826839475
4188228340188228341CA11GENIChomozygous826839476
4188231024188231025TC10GENICheterozygous826839477
4188234517188234525CATACATA--------7GENICheterozygous826839478
4188235226188235227GA18GENICheterozygous826839479
4188236138188236139A-9GENICheterozygous826839480
4188240130188240142GCTGGCTGGCTG------------19GENICheterozygous826839481
4188241329188241330CT22GENICheterozygous826839482
4188241776188241777TC15GENICheterozygous826839483