chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167409839774098398CT22GENIChomozygous112079059
167409884974098850TG15GENIChomozygous112031397
167409998174099982CT13GENIChomozygous112079061
167410056974100570GT17GENIChomozygous112079063
167410058774100588AT17GENIChomozygous111860619
167410172374101724AG15GENIChomozygous111860620
167410189574101896GA16GENIChomozygous112031399
167410223774102238GA9GENIChomozygous112031403
167409950874099509TA17GENICheterozygous119229164
167409975874099759GA18GENIChomozygous119199608
167409982174099822GA14GENIChomozygous119210750
167409985274099853AC12GENIChomozygous112252746
167410261074102610A11GENIChomozygous129381529
167410264374102644AG11GENIChomozygous119199609
167410275674102757AG8GENIChomozygous112361287
167410277074102771TC9GENIChomozygous119199610
167410281374102814CG11GENIChomozygous119210752
167410288074102881CA13GENIChomozygous119199611
167410289574102896AG14GENIChomozygous119129199
167410312474103125TC21GENIChomozygous112031405
167410365174103652GA16GENIChomozygous112031407
167410366274103663AG14GENIChomozygous111860621
167410374574103746GA3GENIChomozygous112031410
167410384774103848AG13GENIChomozygous112031412
167410394374103944AG19GENIChomozygous112031414
167410396874103969TC21GENIChomozygous111860622
167410408674104087GA16GENIChomozygous112079065
167410450774104508AG22GENIChomozygous111860624
167410451074104511CT23GENIChomozygous111860625
167410451274104513AC24GENIChomozygous111860626
167410460574104606GA23GENIChomozygous112031416
167410467274104673GA17GENIChomozygous111860628
167410479074104791GT22GENIChomozygous112031418
167410480674104807GA17GENIChomozygous112079067
167410490474104905CG17GENIChomozygous111860630
167410318974103189TGATGTGCTGTCCTCCCTCCTG16GENIChomozygous131181780
167410323374103233TGATGTGCCGTCCTCCCTCTCG13GENIChomozygous131181781