chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101300765113007652AG43GENIChomozygous138725501
101300784513007846GT38GENIChomozygous138725502
101300803513008036TC48GENIChomozygous138725503
101300879113008792TG49GENIChomozygous138725504
101300891413008915GA58GENIChomozygous138725505
101300895713008958CT62GENIChomozygous138725506
101300902613009027CA51GENIChomozygous138725508
101300903013009031TC50GENIChomozygous138725509
101300903513009036AG50GENIChomozygous138725510
101300903613009037TC49GENIChomozygous138725511
101300906713009067TCTA43GENIChomozygous138668922
101300908213009083GA51GENIChomozygous138725512
101300918413009185TC62GENIChomozygous138725513
101300919113009192GA59GENIChomozygous138725514
101300969413009695AG58GENIChomozygous138725515
101300986513009866GA68GENIChomozygous138725516
101300992213009923TC55GENIChomozygous138725517
101300992913009930TC56GENIChomozygous138725518
101301007713010078AC58GENIChomozygous138725519
101301007813010079CT58GENIChomozygous138725520
101301016313010164GA54GENIChomozygous138725521
101301022013010220GTG49GENIChomozygous138668923
101301022813010229CT53GENIChomozygous138725522
101301026513010266GA50GENIChomozygous138725523
101301043113010432AG54GENIChomozygous138725524
101301043613010438GT53GENIChomozygous138668924
101301117113011172CA46GENIChomozygous142216898
101301062113010622TG65GENIChomozygous138725525
101301095013010951GA47GENIChomozygous138725526
101301110013011101GA47GENIChomozygous142216897
101301121513011216GA54GENIChomozygous142216899
101301197213011973TC42GENIChomozygous142216900
101301222113012222AG46GENIChomozygous142216901
101301223713012238CT43GENIChomozygous142216902
101301324913013250AG41GENIChomozygous142216903
101301325413013255TC39GENIChomozygous142216904
101301360013013601TC49GENIChomozygous142216905
101301374613013747TC44GENIChomozygous138725529
101301459213014593CT41GENIChomozygous142216906
101301259613012602GGGGGT47GENIChomozygous142196550