chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45125895651258957TA3GENIChomozygous56887200
45125896951258970AG5GENIChomozygous56887202
45125946651259467CA14GENICpossibly homozygous56887204
45125953851259539GC11GENICpossibly homozygous56887208
45125954551259547TC--6GENICheterozygous56887210
45125958551259586CT11GENIChomozygous56887212
45125965751259658TG13GENIChomozygous56887215
45125977851259779C-16GENIChomozygous56887217
45125978051259787TACATAC-------19GENIChomozygous56887219
45126019551260196GT16GENIChomozygous56887221
45126072151260722CT25GENICpossibly homozygous56887223
45126112451261125AT9GENICpossibly homozygous56887225
45126127951261280TC22GENIChomozygous56887227
45126154551261546TC10GENIChomozygous56887229
45126244751262448AG18GENICpossibly homozygous56887235
45126263151262632GA17GENICheterozygous56887237
45126263251262633AG18GENICheterozygous56887239
45126342651263427TC17GENIChomozygous56887243
45126573851265739A-1GENIChomozygous58333837
45128734851287349G-2GENICheterozygous58406514
45129439251294393GA11GENIChomozygous56887259
45129830651298307C-7GENICheterozygous56887267
45129831251298313A-6GENICheterozygous56887269
45136387251363873AAG14GENICpossibly homozygous56887311
45136392851363929CT13GENIChomozygous56887313
45136395451363955CT16GENICpossibly homozygous56887315
45136412951364130AACTCTCT3GENICheterozygous58636018