chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4185062870185062871GA42GENIChomozygous655948046
4185064110185064111GA26GENIChomozygous655948047
4185065152185065153TC36GENIChomozygous655948048
4185065755185065757TT--10GENICheterozygous760591517
4185066289185066290CT23GENICpossibly homozygous655948049
4185068446185068447AG32GENIChomozygous655948050
4185068456185068457AG33GENIChomozygous655948051
4185069222185069223CG42GENIChomozygous655948052
4185069649185069650GT24GENIChomozygous655948053
4185070281185070282AG22GENIChomozygous655948054
4185070307185070308CG28GENIChomozygous655948055
4185072618185072619AG13GENIChomozygous655948056
4185072656185072657TC18GENIChomozygous655948057
4185073177185073178GA24GENIChomozygous655948058
4185073953185073954CT42GENIChomozygous655948059
4185074136185074137AG32GENIChomozygous655948060
4185074721185074723CA--4GENIChomozygous760591518
4185076137185076138AT11GENIChomozygous655948061
4185076167185076168GA10GENIChomozygous655948062
4185076433185076434TC10GENIChomozygous655948063
4185076505185076506TC17GENIChomozygous655948064
4185077185185077186GA16GENICpossibly homozygous655948065
4185078616185078617CA25GENIChomozygous655948066
4185078904185078905TG33GENIChomozygous655948067
4185078976185078977CT32GENIChomozygous655948068
4185079888185079889GA26GENIChomozygous655948069
4185080949185080950AG38GENIChomozygous655948070
4185081071185081072GT33GENIChomozygous655948071
4185081477185081478GT24GENIChomozygous655948072
4185081651185081652AC26GENIChomozygous655948073
4185081949185081950TC24GENIChomozygous655948074
4185082690185082691G-22GENIChomozygous760591519
4185084183185084184CT28GENICpossibly homozygous655948075
4185084198185084199AAGTTT18GENICpossibly homozygous760591520
4185084903185084904GA36GENIChomozygous655948076
4185085270185085271TC18GENIChomozygous655948077
4185085328185085329CCGG4GENICheterozygous760591521
4185086602185086603GA24GENIChomozygous655948078
4185087869185087870AG42GENIChomozygous655948079