chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117109153117109154CG59GENIChomozygous115846293
7117111454117111455CA45GENIChomozygous115846295
7117113309117113310TC69GENIChomozygous115846297
7117114234117114235CT51GENIChomozygous115846299
7117114531117114532AG50GENIChomozygous115846301
7117117487117117487C40GENIChomozygous128510446
7117119205117119205CCCTTGCCACAA43GENIChomozygous128510447
7117119260117119261TC42GENIChomozygous115846303
7117122371117122372AG47GENIChomozygous115846305
7117124774117124775AT68GENIChomozygous115846307
7117125664117125665AG58GENIChomozygous115846309
7117125802117125803AG52GENIChomozygous115846311
7117126403117126404GA67GENICpossibly homozygous115846313