chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X115639594115639595CT16GENIChomozygous108312640
X115639829115639830CT15GENIChomozygous108312642
X115639851115639852AC16GENIChomozygous108312644
X115640075115640076TG18GENIChomozygous108312646
X115641265115641266GT2GENIChomozygous108312648
X115666331115666332GA26GENIChomozygous108312650
X115672705115672706GT8GENIChomozygous108312652
X115672720115672721AG11GENIChomozygous108312654
X115672727115672728GA11GENIChomozygous108312656
X115672728115672729TC12GENIChomozygous108312658
X115672729115672730GT12GENIChomozygous108312660
X115672738115672739GC15GENIChomozygous108312662
X115672741115672742TC15GENIChomozygous108312664
X115672745115672746GA15GENIChomozygous108312666
X115672777115672778GT18GENIChomozygous108312668
X115672783115672784GT19GENIChomozygous108312670
X115722661115722662AT10GENICheterozygous108312672
X115722662115722663AG10GENICheterozygous108312674
X115761816115761817AT19GENIChomozygous108312676
X115761817115761818TA19GENIChomozygous108312678
X115774512115774513GC21GENIChomozygous108312680
X115866973115866974AC12GENIChomozygous108312682
X115866976115866977AG11GENIChomozygous108312684
X115866979115866980AT11GENIChomozygous108312686
X115866980115866981AC11GENIChomozygous108312688