chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45125895651258957TA7GENICheterozygous562493677
45125896951258970AG3GENIChomozygous562493678
45125946651259467CA10GENICheterozygous562493679
45125953851259539GC4GENICheterozygous562493680
45125954551259547TC--2GENIChomozygous708220766
45125965751259658TG10GENIChomozygous562493681
45125977851259779C-11GENICpossibly homozygous708220767
45125978051259787TACATAC-------15GENICpossibly homozygous708220768
45126019551260196GT29GENICpossibly homozygous564973509
45126072151260722CT20GENICpossibly homozygous564973510
45126112451261125AT11GENICpossibly homozygous564973511
45126127951261280TC13GENIChomozygous564973512
45126154551261546TC20GENICpossibly homozygous562493682
45126244751262448AG27GENIChomozygous562493683
45126263151262632GA23GENICheterozygous564973513
45126263251262633AG23GENICheterozygous564973514
45126342651263427TC17GENIChomozygous562493684
45126568351265684A-2GENIChomozygous708220769
45126573851265739A-3GENICheterozygous708220771
45129439251294393GA16GENIChomozygous562493685
45129830651298307C-8GENIChomozygous708220774
45129831251298313A-10GENICpossibly homozygous708220775
45136000151360003AC--1GENIChomozygous708220777
45136387251363873AAG14GENIChomozygous708220779
45136392851363929CT11GENICpossibly homozygous562493686
45136395451363955CT13GENICheterozygous562493687