chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109917277109917278AG28GENIChomozygous54628006
6109917488109917489GT27GENIChomozygous54628008
6109917937109917938CT10GENIChomozygous55096585
6109918006109918007TC18GENIChomozygous55096587
6109918503109918504GGTGC26GENIChomozygous54628012
6109919051109919052CT21GENIChomozygous54628014
6109919174109919180AGAGAG------4GENIChomozygous55528921
6109920957109920958AC21GENIChomozygous54943398
6109921079109921080GA15GENIChomozygous54628022
6109921138109921139GC21GENIChomozygous55096589
6109921748109921760GTGTGTGTGTGT------------12GENICheterozygous55528923
6109921750109921760GTGTGTGTGT----------12GENICpossibly homozygous55528925
6109923146109923147TTTATTTGTA33INTERGENIChomozygous54628034
6109923291109923292TC27INTERGENIChomozygous54628036
6109924456109924457GA29INTERGENIChomozygous54943403
6109924468109924472TTGT----21INTERGENIChomozygous54628038
6109925472109925473TC36INTERGENIChomozygous54628046
6109926368109926369AT22INTERGENIChomozygous54628048
6109927387109927388CT23INTERGENIChomozygous55096593
6109927396109927397AG20INTERGENIChomozygous55096595
6109928230109928231TTGTAGTAGTAGTAGTA7INTERGENIChomozygous55528927
6109929204109929206TT--14INTERGENIChomozygous55096597
6109929207109929208AC14INTERGENIChomozygous55528929
6109930268109930269TC30INTERGENIChomozygous55096599
6109931009109931010AAT14INTERGENICpossibly homozygous55048506
6109932728109932729GA19INTERGENIChomozygous54628060
6109932784109932785TTAGTAGA11INTERGENIChomozygous55528931
6109933008109933009G-11INTERGENIChomozygous54628070
6109934637109934638CT29INTERGENIChomozygous54628072
6109936178109936179AT33INTERGENIChomozygous54628076