chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4185062870185062871GA11GENIChomozygous648346566
4185064110185064111GA17GENIChomozygous648346567
4185065152185065153TC26GENIChomozygous648346568
4185065755185065757TT--8GENICpossibly homozygous756089092
4185066289185066290CT15GENIChomozygous648346569
4185068446185068447AG17GENIChomozygous648346570
4185068456185068457AG15GENIChomozygous648346571
4185069222185069223CG21GENIChomozygous648346572
4185069649185069650GT15GENIChomozygous648346573
4185070281185070282AG27GENIChomozygous648346574
4185070307185070308CG26GENIChomozygous648346575
4185072618185072619AG19GENIChomozygous648346576
4185072656185072657TC25GENIChomozygous648346577
4185073177185073178GA27GENIChomozygous648346578
4185073953185073954CT17GENIChomozygous648346579
4185074136185074137AG29GENIChomozygous648346580
4185074721185074723CA--2GENIChomozygous756089093
4185076137185076138AT9GENIChomozygous648346581
4185076167185076168GA12GENIChomozygous648346582
4185076433185076434TC7GENIChomozygous648346583
4185076505185076506TC3GENIChomozygous648346584
4185077185185077186GA34GENIChomozygous648346585
4185078616185078617CA18GENIChomozygous648346586
4185078904185078905TG6GENIChomozygous648346587
4185078976185078977CT12GENIChomozygous648346588
4185079888185079889GA19GENIChomozygous648346589
4185080949185080950AG16GENIChomozygous648346590
4185081071185081072GT13GENIChomozygous648346591
4185081477185081478GT17GENICpossibly homozygous648346592
4185081651185081652AC23GENIChomozygous648346593
4185081949185081950TC24GENIChomozygous648346594
4185082690185082691G-17GENIChomozygous756089094
4185084183185084184CT21GENIChomozygous648346595
4185084198185084199AAGTTT24GENIChomozygous756089095
4185084903185084904GA23GENIChomozygous648346596
4185085270185085271TC16GENIChomozygous648346597
4185085328185085329CCGG3GENICheterozygous756089096
4185086602185086603GA27GENIChomozygous648346598
4185087869185087870AG25GENIChomozygous648346599