chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1220762831220762832AG26GENIChomozygous108543032
1220763296220763297CA41GENIChomozygous108994468
1220764396220764397CG25GENIChomozygous108994469
1220764463220764464TC34GENIChomozygous108543040
1220765531220765532GA32GENIChomozygous108994470
1220766341220766342GA37GENIChomozygous108994471
1220766571220766572GA40GENIChomozygous108994472
1220766576220766577GA38GENICpossibly homozygous108994473
1220766766220766767TC23GENIChomozygous108543046
1220767694220767695TC26GENIChomozygous108994474
1220768516220768517TA32GENIChomozygous108543050
1220768787220768788AG31GENIChomozygous108543054
1220769127220769128TC12GENIChomozygous108543060
1220771089220771090TA28GENIChomozygous108994475