chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X11729701172971CG39GENIChomozygous149461759
X11732531173254CT21GENIChomozygous149461760
X11734141173415CG22GENIChomozygous147224225
X11774571177458AG43GENIChomozygous149461761
X11819171181918CA17GENIChomozygous140602087
X11826571182658GA30GENIChomozygous149461762
X11829321182933A5GENICheterozygous403473482
X11829321182933AT5GENICheterozygous403473483
X11829381182939A6GENICheterozygous403473488
X11829381182939AT6GENICheterozygous403473489
X11860721186073GA5GENICheterozygous404803497
X11860801186081GA6GENICheterozygous404803498
X11915381191539GA26GENIChomozygous149461763
X11919261191927GA23GENIChomozygous149461764
X11937851193786A9GENICheterozygous404449574
X11860541186055GA5GENICheterozygous145101502
X11860881186089GA7GENICheterozygous145101503
X11860601186061GA4GENICheterozygous148992013
X11934211193422TC11GENICheterozygous404449570
X11934211193422T11GENICpossibly homozygous404449571
X11934271193428TC11GENICheterozygous404449572
X11934271193428T11GENICpossibly homozygous404449573
X11937851193786AT9GENICheterozygous404449575
X11937871193788AT13GENICheterozygous149461765
X12171371217138GA33GENIChomozygous149461766
X11861031186104G6GENIChomozygous149456058
X11986021198603AG28GENIChomozygous140602092
X12057981205799AG21GENIChomozygous140602093
X12073691207370GT24GENICheterozygous145225175
X12073891207390CT30GENICheterozygous145225176
X12073981207399GA30GENICheterozygous145225177
X11937871193788A13GENICheterozygous404829949
X12175981217599AC40GENIChomozygous140602101
X12181841218185TC31GENIChomozygous140602102
X12192841219285TC26GENIChomozygous149461767
X12231811223182GA29GENIChomozygous140602104
X12269421226943CG27GENIChomozygous149461768