chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2226468394226468395TC16GENIChomozygous59420502
2226468988226468989TC24GENIChomozygous59420504
2226469387226469389AA--11GENIChomozygous59420506
2226469490226469491AG22GENIChomozygous59420508
2226470045226470046GA8GENICpossibly homozygous59420510
2226470367226470368TC29GENIChomozygous59420511
2226470379226470380AG27GENIChomozygous59420513
2226470822226470826AGAG----1GENIChomozygous59775418
2226470873226470874AG8GENIChomozygous59420515
2226470874226470875AC5GENIChomozygous59420517
2226472968226472969GA17GENICpossibly homozygous59420519
2226473031226473032A-13GENIChomozygous59420521
2226473731226473732CG18GENIChomozygous59420523
2226474523226474524AAT15GENICpossibly homozygous59420525
2226475566226475567CT30GENIChomozygous59420527
2226475788226475789GA36GENIChomozygous59420529
2226476524226476525AG22GENIChomozygous59420531
2226476652226476653AG24GENIChomozygous59420533
2226476811226476812AG22GENIChomozygous59420535
2226476944226476945GT22GENICpossibly homozygous59420537
2226476945226476946CT22GENIChomozygous59420539
2226477216226477217TC20GENIChomozygous59420541