chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1811465341146535TC60GENIChomozygous110512404
1811475241147525GA42GENIChomozygous110512406
1811492351149236GA59GENIChomozygous110512408
1811502121150213GA47GENIChomozygous119577900
1811502141150215AT48GENIChomozygous119509952
1811502151150216AG48GENIChomozygous119577901
1811502231150224TC48GENIChomozygous119509954
1811502441150245GT46GENIChomozygous119509956
1811518001151801TC51GENIChomozygous110568922
1811518181151819TC47GENIChomozygous110568925
1811531121153113AG53GENIChomozygous110640989
1811540811154082CT45GENIChomozygous110512410
1811558641155865CG51GENIChomozygous110512412
1811577711157772AC52GENIChomozygous110512415
1811586541158655AT46GENIChomozygous110512417
1811599241159925CT53GENIChomozygous110512419
1811612741161275GA63GENIChomozygous110512422
1811661571166158GC47GENIChomozygous110512424
1811662901166291GA39GENIChomozygous110512426
1811665731166574TC57GENIChomozygous119509958
1811668301166831TC61GENIChomozygous119509966
1811682841168285GT49GENIChomozygous110512428
1811704901170491TG65GENIChomozygous110512430
1811726371172638GA59GENIChomozygous110512432
1811752231175223TTTCAGA57GENIChomozygous131202386
1811532231153223TAATCT52GENIChomozygous131202381
1811550321155033T44GENIChomozygous131202382
1811603081160308C63GENICpossibly homozygous132225064
1811761011176102GA57GENIChomozygous110512436