chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4188175714188175715CG10GENICheterozygous57565980
4188178331188178332CCA19GENIChomozygous57027395
4188179922188179923AAAC7GENICheterozygous57565984
4188180500188180501AG8GENICheterozygous57565986
4188187186188187187GGT12GENICheterozygous57565998
4188194677188194678AG19GENICheterozygous57566002
4188195186188195187CA10GENICheterozygous57566004
4188200472188200473GA11GENICheterozygous57566006
4188205452188205453CT10GENICheterozygous57027400
4188205458188205459GA10GENICheterozygous57027401
4188205459188205460GA10GENICheterozygous57027402
4188205490188205492AA--14GENICheterozygous57027403
4188205495188205496GA14GENICheterozygous60053911
4188206584188206585CCA24GENIChomozygous57027404
4188207943188207944GA13GENICheterozygous57566012
4188218451188218452GGA10GENIChomozygous57027407
4188228328188228329CA8GENIChomozygous57027408
4188228335188228336CA10GENIChomozygous57027409
4188228340188228341CA11GENIChomozygous57027410
4188231024188231025TC10GENICheterozygous57566024
4188234517188234525CATACATA--------7GENICheterozygous58484366
4188235226188235227GA18GENICheterozygous57566032
4188236138188236139A-9GENICheterozygous57566033
4188240130188240142GCTGGCTGGCTG------------19GENICheterozygous57566039
4188241329188241330CT22GENICheterozygous57566045
4188241776188241777TC15GENICheterozygous57566047