chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4185062870185062871GA16GENIChomozygous652143796
4185064110185064111GA25GENIChomozygous652143797
4185065152185065153TC24GENIChomozygous652143798
4185065755185065757TT--8GENICheterozygous758325027
4185065774185065779GGTTC-----9GENICheterozygous758325028
4185066289185066290CT24GENIChomozygous652143799
4185068446185068447AG26GENIChomozygous652143800
4185068456185068457AG25GENIChomozygous652143801
4185069222185069223CG25GENIChomozygous652143802
4185069649185069650GT26GENIChomozygous652143803
4185070281185070282AG20GENIChomozygous652143804
4185070307185070308CG22GENIChomozygous652143805
4185072618185072619AG16GENIChomozygous652143806
4185072656185072657TC7GENIChomozygous652143807
4185073177185073178GA17GENIChomozygous652143808
4185073953185073954CT19GENIChomozygous652143809
4185074136185074137AG29GENIChomozygous652143810
4185074721185074723CA--3GENICheterozygous758325029
4185076137185076138AT25GENIChomozygous652143811
4185076167185076168GA18GENIChomozygous652143812
4185076433185076434TC13GENIChomozygous652143813
4185076505185076506TC16GENIChomozygous652143814
4185077185185077186GA20GENIChomozygous652143815
4185078616185078617CA15GENIChomozygous652143816
4185078904185078905TG21GENIChomozygous652143817
4185078976185078977CT24GENIChomozygous652143818
4185079888185079889GA17GENIChomozygous652143819
4185080949185080950AG22GENIChomozygous652143820
4185081071185081072GT18GENIChomozygous652143821
4185081477185081478GT19GENIChomozygous652143822
4185081651185081652AC20GENIChomozygous652143823
4185081949185081950TC16GENIChomozygous652143824
4185082690185082691G-16GENIChomozygous758325030
4185084183185084184CT18GENIChomozygous652143825
4185084198185084199AAGTTT16GENIChomozygous758325031
4185084903185084904GA18GENIChomozygous652143826
4185085270185085271TC23GENIChomozygous652143827
4185085328185085329CCGG1GENIChomozygous758325032
4185086602185086603GA18GENIChomozygous652143828
4185087869185087870AG24GENIChomozygous652143829