chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2251454564251454565AT13GENIChomozygous111037063
2251455189251455190GA9GENIChomozygous111037065
2251455521251455522CT13GENIChomozygous111037067
2251456074251456075GA11GENIChomozygous111037069
2251456275251456276GA21GENIChomozygous111037071
2251456558251456559GC8GENIChomozygous110384627
2251458748251458749CA16GENIChomozygous110384631
2251459062251459063GT8GENIChomozygous110384633
2251461975251461976AG21GENIChomozygous110384639
2251462649251462650GA10GENIChomozygous111037073
2251463550251463551GA16GENIChomozygous111037075
2251464338251464339GA16GENIChomozygous111037077
2251464950251464951TG11GENIChomozygous111037079
2251465732251465733GA21GENICheterozygous110384643
2251465787251465788CT8GENICheterozygous110384651
2251465897251465898CA12GENIChomozygous111037081
2251466044251466045CT15GENIChomozygous110384653
2251467280251467281CG18GENIChomozygous111037087
2251469032251469033TG7GENIChomozygous111037089
2251469398251469399GC14GENIChomozygous111037091
2251470413251470414CT16GENIChomozygous111037093
2251471690251471691AG21GENIChomozygous110384674
2251474155251474156AG12GENIChomozygous110384682
2251475098251475099AT21GENIChomozygous111037095
2251476561251476562AG19GENIChomozygous110384688
2251478785251478786AG11GENIChomozygous110384696
2251480546251480547AG11GENIChomozygous110384702
2251481886251481887AG12GENIChomozygous110384706
2251484074251484075TC18GENIChomozygous110384712
2251484503251484504AG16GENIChomozygous110384714
2251484755251484756AG14GENIChomozygous110384716