chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101057520610575207TC29GENICpossibly homozygous116493315
101057549610575497TC9GENIChomozygous116493317
101057599710575998GA38GENIChomozygous116493319
101057623410576235CT27GENIChomozygous116493321
101057651810576519CT18GENIChomozygous116493323
101057844610578447CT13GENIChomozygous116493325
101057947110579472AC34GENIChomozygous116493327
101057961410579615AG23GENIChomozygous116493329
101058011410580115AG24GENIChomozygous116734006
101058083910580840AC30GENIChomozygous116493331