chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4185062870185062871GA27GENIChomozygous644542711
4185064110185064111GA28GENIChomozygous644542712
4185065152185065153TC27GENIChomozygous644542713
4185065755185065757TT--5GENICheterozygous753795710
4185065774185065779GGTTC-----18GENICheterozygous753795711
4185066289185066290CT29GENIChomozygous644542714
4185068446185068447AG30GENIChomozygous644542715
4185068456185068457AG27GENIChomozygous644542716
4185069222185069223CG36GENIChomozygous644542717
4185069649185069650GT26GENICpossibly homozygous644542718
4185070281185070282AG33GENIChomozygous644542719
4185070307185070308CG30GENIChomozygous644542720
4185072618185072619AG23GENIChomozygous644542721
4185072656185072657TC21GENIChomozygous644542722
4185073177185073178GA27GENIChomozygous644542723
4185073953185073954CT20GENIChomozygous644542724
4185074136185074137AG27GENICpossibly homozygous644542725
4185074721185074723CA--5GENIChomozygous753795712
4185076137185076138AT15GENIChomozygous644542726
4185076167185076168GA15GENIChomozygous644542727
4185076433185076434TC22GENIChomozygous644542728
4185076505185076506TC23GENIChomozygous644542729
4185077185185077186GA34GENIChomozygous644542730
4185078616185078617CA23GENICpossibly homozygous644542731
4185078904185078905TG21GENIChomozygous644542732
4185078976185078977CT29GENIChomozygous644542733
4185079888185079889GA27GENIChomozygous644542734
4185080949185080950AG23GENIChomozygous644542735
4185081071185081072GT28GENIChomozygous644542736
4185081477185081478GT25GENIChomozygous644542737
4185081651185081652AC26GENIChomozygous644542738
4185081949185081950TC31GENIChomozygous644542739
4185082690185082691G-35GENIChomozygous753795713
4185084183185084184CT21GENIChomozygous644542740
4185084198185084199AAGTTT19GENIChomozygous753795714
4185084903185084904GA34GENIChomozygous644542741
4185085270185085271TC16GENIChomozygous644542742
4185085328185085329CCGG6GENIChomozygous753795715
4185086602185086603GA25GENIChomozygous644542743
4185087869185087870AG19GENIChomozygous644542744