chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4144003677144003678CT24GENIChomozygous56963692
4144004239144004240AG28GENIChomozygous59246834
4144004815144004816TC29GENIChomozygous56963694
4144005846144005847AG20GENIChomozygous56963701
4144006388144006389CT21GENIChomozygous56963702
4144008159144008160TA31GENIChomozygous56963709
4144008359144008360TA27GENIChomozygous59246836
4144008585144008586TTAAGC7GENIChomozygous56963710
4144009387144009388AG37GENIChomozygous56963712
4144009860144009861TA24GENIChomozygous59246838
4144011159144011160GT16GENIChomozygous56963714
4144012104144012105GA21GENIChomozygous56963722
4144012107144012108A-21GENIChomozygous56963723
4144012810144012811AG24GENIChomozygous56963730
4144013391144013392TC19GENIChomozygous59246840
4144014184144014185CT24GENIChomozygous59246842
4144014387144014388GA23GENIChomozygous59246844
4144014857144014858GA18GENIChomozygous59246846
4144015020144015021CT15GENIChomozygous59246848
4144015417144015418GC31GENIChomozygous56963738
4144015977144015978AG36GENIChomozygous59246850
4144017238144017239GT8GENIChomozygous59246852
4144018321144018322AAT37GENICpossibly homozygous56963751
4144018338144018339GA43GENICpossibly homozygous59246854
4144014750144014751TTATAC14GENICpossibly homozygous57342529
4144021790144021791CT22GENIChomozygous59246856
4144024508144024509CT22GENIChomozygous59246858
4144024607144024608AC23GENIChomozygous59246860
4144025544144025545CCA24GENIChomozygous59246862
4144026264144026265CA28GENIChomozygous56963784
4144027877144027878A-33GENIChomozygous59246864