chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117107189117107190GA21GENIChomozygous116301972
7117108447117108448TC12GENIChomozygous116301973
7117109153117109154CG12GENIChomozygous115846293
7117109251117109252CT15GENIChomozygous116301974
7117111454117111455CA8GENIChomozygous115846295
7117111674117111675GA16GENIChomozygous116301975
7117114234117114235CT21GENIChomozygous115846299
7117114531117114532AG15GENIChomozygous115846301
7117116950117116951CT25GENIChomozygous116301976
7117119260117119261TC16GENIChomozygous115846303
7117122371117122372AG18GENIChomozygous115846305
7117124774117124775AT18GENIChomozygous115846307
7117125664117125665AG12GENIChomozygous115846309
7117125802117125803AG21GENIChomozygous115846311
7117127353117127354TC19GENIChomozygous116301977
7117127582117127582AAC10GENIChomozygous131023954
7117117487117117487C15GENIChomozygous128510446
7117119205117119205CCCTTGCCACAA15GENIChomozygous128510447