chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55655520956555210CA16GENIChomozygous775282360
55655563956555640GC47GENIChomozygous775282361
55655610056556101TG57GENICpossibly homozygous775282362
55655687156556872AC48GENIChomozygous775282363
55655739456557395TC48GENIChomozygous775282364
55655883856558839AT28GENIChomozygous775282365
55655903656559037AG29GENIChomozygous775282366
55655949856559499AT44GENIChomozygous775282367
55655986656559867TC32GENIChomozygous775282368
55656006956560070GA24GENICheterozygous775282369
55656016356560164CT29GENICheterozygous775282370
55656078356560784AG30GENICheterozygous775282371
55656079556560796CT34GENICheterozygous775282372
55656080256560803CT33GENICheterozygous775282373
55656093156560932CT42GENIChomozygous775282374
55656100456561005AG46GENIChomozygous775282375
55656114056561141GT15GENIChomozygous775282376
55656208056562081CT32GENICpossibly homozygous775282377
55656254656562547TC20GENIChomozygous775282378
55656318756563188TC63GENIChomozygous775282379
55656330756563308TA44GENIChomozygous775282380
55656435356564354CA36GENIChomozygous775282381
55656514356565144TG30GENIChomozygous775282382
55656521156565212AG27GENIChomozygous775282383
55656583756565838CT29GENIChomozygous775282384
55656616956566170TC46GENIChomozygous775282385
55656621356566214GA36GENICpossibly homozygous775282386