chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35279190852791909TC22GENIChomozygous71888517
35279291652792917TC18GENIChomozygous71888521
35279732752797328AG23GENICheterozygous71888528
35279788952797890TC25GENIChomozygous71888530
35280076852800769AG21GENIChomozygous71888535
35280121452801215AG20GENIChomozygous71888536
35280121652801217AG20GENIChomozygous71888537
35279719552797196AG11GENIChomozygous72361025
35280253852802539TG28GENICheterozygous71888538
35280479752804798TC25GENIChomozygous71888543
35281379552813796AG14GENICheterozygous72361028
35281379852813799GA14GENICpossibly homozygous71888567
35281381552813816GA15GENICheterozygous72361031
35281383552813836AG17GENICheterozygous72361034
35281400952814010TG23GENICheterozygous71888570
35281767252817673TC28GENIChomozygous71888578
35281769352817694CT29GENIChomozygous72361037
35281784952817850GA26GENIChomozygous71888579
35281817252818173GT19GENIChomozygous72361040
35282021452820215CT25GENIChomozygous71888587
35282197352821974AC13GENIChomozygous71888590
35282198352821984GC16GENIChomozygous71888591
35282201952822020AT17GENIChomozygous71888592
35282572752825728TC20GENIChomozygous72361043
35282669852826699TG24GENICheterozygous72361046
35282746152827462TG22GENIChomozygous71888598
35282898052828981GA17GENIChomozygous71888600
35282924452829245GA15GENIChomozygous71888601
35282928952829290TC24GENIChomozygous71888602