chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167409839774098398CT65GENIChomozygous112079059
167409884974098850TG67GENIChomozygous112031397
167409975874099759GA15GENIChomozygous119199608
167409982174099822GA9GENIChomozygous119210750
167409985274099853AC13GENIChomozygous112252746
167409998174099982CT38GENIChomozygous112079061
167410056974100570GT57GENIChomozygous112079063
167410058774100588AT56GENIChomozygous111860619
167410172374101724AG46GENIChomozygous111860620
167410189574101896GA56GENIChomozygous112031399
167410223774102238GA39GENIChomozygous112031403
167410264374102644AG30GENIChomozygous119199609
167410275674102757AG29GENIChomozygous112361287
167410277074102771TC30GENIChomozygous119199610
167410281374102814CG25GENIChomozygous119210752
167410288074102881CA42GENIChomozygous119199611
167410289574102896AG43GENIChomozygous119129199
167410312474103125TC33GENIChomozygous112031405
167410318974103189TGATGTGCTGTCCTCCCTCCTG32GENIChomozygous131181780
167410323374103233TGATGTGCCGTCCTCCCTCTCG40GENIChomozygous131181781
167410365174103652GA32GENIChomozygous112031407
167410366274103663AG26GENIChomozygous111860621
167410374574103746GA16GENIChomozygous112031410
167410384774103848AG45GENIChomozygous112031412
167410394374103944AG53GENIChomozygous112031414
167410396874103969TC53GENIChomozygous111860622
167410408674104087GA47GENIChomozygous112079065
167410450774104508AG52GENIChomozygous111860624
167410451074104511CT50GENIChomozygous111860625
167410451274104513AC49GENIChomozygous111860626
167410460574104606GA49GENIChomozygous112031416
167410467274104673GA66GENIChomozygous111860628
167410479074104791GT47GENIChomozygous112031418
167410480674104807GA53GENIChomozygous112079067
167410490474104905CG55GENIChomozygous111860630
167410261074102610A29GENIChomozygous129381529
167410008074100092ACCAACAACAAC5GENICheterozygous132207737