chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2251454564251454565AT18GENIChomozygous111037063
2251455189251455190GA26GENIChomozygous111037065
2251455521251455522CT14GENIChomozygous111037067
2251456074251456075GA14GENIChomozygous111037069
2251456275251456276GA15GENIChomozygous111037071
2251456558251456559GC18GENIChomozygous110384627
2251458748251458749CA20GENIChomozygous110384631
2251459062251459063GT13GENIChomozygous110384633
2251461975251461976AG29GENIChomozygous110384639
2251462649251462650GA27GENIChomozygous111037073
2251463550251463551GA16GENIChomozygous111037075
2251464338251464339GA34GENIChomozygous111037077
2251464950251464951TG21GENIChomozygous111037079
2251465732251465733GA24GENICheterozygous110384643
2251465897251465898CA16GENIChomozygous111037081
2251466044251466045CT11GENIChomozygous110384653
2251467065251467066CA11GENIChomozygous111037085
2251467280251467281CG16GENIChomozygous111037087
2251469032251469033TG23GENICpossibly homozygous111037089
2251469398251469399GC25GENIChomozygous111037091
2251470413251470414CT25GENIChomozygous111037093
2251471690251471691AG20GENIChomozygous110384674
2251474155251474156AG31GENIChomozygous110384682
2251475098251475099AT22GENIChomozygous111037095
2251476561251476562AG12GENIChomozygous110384688
2251477043251477044TC2GENIChomozygous111037097
2251478785251478786AG10GENIChomozygous110384696
2251480546251480547AG24GENIChomozygous110384702
2251481455251481456TC11GENIChomozygous110384704
2251481588251481589CA15GENICheterozygous111391044
2251481886251481887AG26GENIChomozygous110384706
2251484074251484075TC16GENIChomozygous110384712
2251484503251484504AG18GENIChomozygous110384714
2251484755251484756AG15GENIChomozygous110384716
2251481590251481591CA13GENICheterozygous120255261