chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3123859109123859110GA25GENIChomozygous58184629
3123863264123863265GA23GENIChomozygous58184631
3123863801123863802GA22GENIChomozygous57647530
3123864445123864446TC35GENIChomozygous57647534
3123866758123866759GA19GENIChomozygous57647538
3123866819123866820GT16GENIChomozygous58184633
3123866926123866927TTC20GENICpossibly homozygous58184635
3123867093123867094AT31GENIChomozygous57647540
3123867646123867647AAGT10GENICheterozygous57647542
3123867646123867647AAGTGT10GENICheterozygous57647544
3123867886123867887GA20GENIChomozygous58184637
3123868723123868724TG29GENICheterozygous57647546
3123868980123868981GGCA22GENIChomozygous58184639
3123870006123870007AG24GENIChomozygous57647552
3123871704123871705TC25GENIChomozygous58184641
3123875207123875208AAC26GENIChomozygous57647570
3123875266123875267GGT21GENIChomozygous57647572
3123876193123876197AACA----17GENIChomozygous58184643
3123876417123876418AG16GENIChomozygous58184645