chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
67773535877735359CT34GENIChomozygous114865086
67773552777735528TC26GENIChomozygous114865087
67773577177735772GT26GENIChomozygous115260344
67773610077736101TC26GENIChomozygous114865089
67773632577736326CT23GENIChomozygous114865090
67773651577736516TC27GENIChomozygous114865091
67773696977736970TC28GENIChomozygous115260346
67773729777737298TC20GENIChomozygous114865093
67773783777737838CT21GENICpossibly homozygous115260348
67773811177738112TG33GENIChomozygous114865096
67773921877739219AC27GENIChomozygous115260350
67773982677739827CT17GENIChomozygous115260352
67774079077740791AC22GENIChomozygous115260354
67774092377740924TC28GENIChomozygous115260356
67774130877741309CT26GENIChomozygous114865102
67774217577742176GA24GENIChomozygous114865108
67774280977742810TG25GENIChomozygous115260360
67774301977743020CT24GENIChomozygous115260362
67774372277743723CT17GENIChomozygous115260364
67774229477742295AC7GENIChomozygous118574273
67774421477744215CT20GENIChomozygous114865112
67774474977744750CT29GENIChomozygous115260366
67774529677745297TA26GENIChomozygous115260368
67774562277745623AG13GENIChomozygous115260370
67774623177746232AT29GENIChomozygous115260372
67774746277747463TC27GENICpossibly homozygous115260374
67774862377748624GA26GENIChomozygous114865121
67774953977749540GA13GENIChomozygous115260376
67774956077749561GA12GENIChomozygous115260378
67774972077749721AG31GENIChomozygous114865122
67774996877749969CT34GENIChomozygous115260382
67775102677751027AC25GENIChomozygous115260384
67775122877751229AT15GENICpossibly homozygous118616272