chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X122940267122940268GC14GENIChomozygous125144588
X122941650122941651GA16GENIChomozygous125116421
X122942333122942334TC11GENIChomozygous125116422
X122943780122943781TC19GENIChomozygous125116423
X122944869122944870GT16GENIChomozygous125116424
X122944975122944976CT16GENIChomozygous125116425
X122945117122945118GC25GENIChomozygous125144594
X122945595122945596AG21GENIChomozygous125116426
X122945677122945678TC15GENIChomozygous125116427
X122947155122947156AT19GENIChomozygous125116428
X122947215122947216GC24GENIChomozygous125116429
X122947495122947496AC20GENIChomozygous125116431
X122947717122947718TC11GENIChomozygous125116432
X122948905122948906AG13GENIChomozygous125116433
X122950548122950549CT8GENIChomozygous125126809
X122950771122950772CT15GENIChomozygous125116435
X122952827122952828CT15GENIChomozygous125116436
X122953371122953372CT18GENIChomozygous125116437
X122953445122953446GA18GENIChomozygous125116438
X122953496122953497TA10GENIChomozygous125144596
X122954163122954164GA17GENIChomozygous125116439
X122956103122956104CT16GENIChomozygous125116440
X122957458122957459TC6GENICheterozygous125144597
X122958325122958326AC25GENIChomozygous125116441
X122959269122959270TC16GENIChomozygous125116442
X122959697122959698AG11GENIChomozygous125116444
X122959801122959802TC9GENIChomozygous125144598
X122962599122962600AG13GENIChomozygous125116446
X122963395122963396GT11GENIChomozygous125144600
X122967694122967695GT19GENIChomozygous125116448
X122971930122971931TG12GENIChomozygous125144603
X122968057122968058CT29GENIChomozygous125116449
X122969616122969617TC19GENIChomozygous125116451
X122970177122970178GA15GENIChomozygous125144601
X122971095122971096TC28GENIChomozygous125144602
X122953241122953242CG13GENIChomozygous125135882
X122972988122972989GC17GENIChomozygous125144605