chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X135010654135010655AC22GENIChomozygous108509489
X135011648135011649TA10GENIChomozygous108818840
X135012103135012104TC7GENIChomozygous108509491
X135013852135013853GA13GENIChomozygous108509493
X135016733135016734TC10GENIChomozygous108509495
X135017871135017872GC14GENIChomozygous108509497
X135019309135019310TG7GENIChomozygous108509499
X135030650135030651TC10GENIChomozygous108818841
X135030651135030652AT10GENIChomozygous108818842
X135031463135031464TC14GENIChomozygous108509503
X135031466135031467GA14GENIChomozygous108509505
X135031472135031473GA13GENIChomozygous108509507
X135031541135031542TG16GENIChomozygous108509509
X135031790135031791GA15GENIChomozygous108509511
X135032779135032780AT14GENIChomozygous108509513
X135032951135032952TA13GENIChomozygous108509515
X135035289135035290AG15GENIChomozygous108509517
X135036004135036005AT14GENIChomozygous108509519
X135038709135038710GA16GENIChomozygous108509521
X135038832135038833GA9GENIChomozygous108509523
X135039233135039234AG13GENIChomozygous108509525
X135039795135039796AC15GENIChomozygous108509527
X135024337135024338CT18GENIChomozygous108815535