chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2031761633176164AG48GENIChomozygous109068219
2031776273177628AT62GENIChomozygous109068221
2031790723179073AG45GENIChomozygous109068223
2031791403179141TC51GENIChomozygous109068225
2031763283176329CT24GENIChomozygous109388852
2031785383178539GA58GENIChomozygous109388853
2031792413179242GA52GENIChomozygous109388854
2031768203176821CG48GENICpossibly homozygous109454609
2031779603177961GA54GENICpossibly homozygous109454612
2031793783179379AG70GENICheterozygous119856526
2031794783179479GA56GENICheterozygous119856527
2031794993179500TC56GENIChomozygous119843710
2031794953179496GA56GENICheterozygous119843709
2031794013179402TC70GENICheterozygous119843708
2031795033179504GA55GENICheterozygous119843711
2031795083179509GA58GENICheterozygous119843712
2031795173179518GA64GENICheterozygous119843713
2031795593179560TC75GENICheterozygous119843714
2031795903179591TC82GENICheterozygous119843715
2031797433179744TC102GENICheterozygous119843717
2031798493179850TC49GENICheterozygous119843718
2031798703179871GT47GENICheterozygous119843719
2031798723179873CT47GENICheterozygous119843720
2031798943179895CT50GENICheterozygous119843721
2031799213179922GC56GENICheterozygous119843722
2031799323179933AG57GENICheterozygous119843723
2031799463179947CT61GENICheterozygous119856528
2031799663179967GA65GENICheterozygous124621723
2031799833179984AC66GENICheterozygous119843724
2031800123180013CT65GENICheterozygous119843725
2031800303180031CT67GENICheterozygous119856529
2031800353180036CG67GENICheterozygous119856530
2031801083180109AG46GENIChomozygous109068227
2031805593180560GT65GENIChomozygous109547270
2031807723180773TC55GENICpossibly homozygous119755920
2031807383180739T57GENICpossibly homozygous129650636
2031799533179956GGT62GENICheterozygous131226909
2031807873180788GA54GENICpossibly homozygous119755921
2031807903180791AG54GENICpossibly homozygous119755922
2031807923180793AC52GENICpossibly homozygous119755923
2031808063180807TC48GENICpossibly homozygous109576016