chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7113206924113206925T37GENICpossibly homozygous141922789
7113208880113208902GACCCTGGAGTGCCATCCTCCG51GENIChomozygous145610473
7113209970113209971CT44GENIChomozygous145636150
7113215763113215764GT29GENIChomozygous145636151
7113215989113215989GC2GENIChomozygous145610474
7113215991113215992CG2GENIChomozygous145636152
7113215993113215994CG3GENIChomozygous142008816
7113218258113218259CT36GENIChomozygous145636153
7113218511113218512GA55GENIChomozygous145636154