chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1234460998234460999CT49GENIChomozygous135836237
1234461184234461186TG45GENIChomozygous135466334
1234461198234461199GC47GENIChomozygous135836238
1234461217234461218AG48GENIChomozygous135836239
1234461238234461239GA41GENIChomozygous135836240
1234461242234461243TG42GENIChomozygous135836241
1234461298234461298A41GENICpossibly homozygous135466335
1234461324234461325CT44GENIChomozygous135836242
1234461355234461356TC46GENIChomozygous135836243
1234461442234461443CT41GENIChomozygous135836244
1234461610234461611TC30GENIChomozygous135836245
1234461715234461716CT31GENIChomozygous135836246
1234461723234461724CT31GENIChomozygous135836247
1234462326234462327CG49GENIChomozygous135836252
1234461741234461742AG27GENIChomozygous135836248
1234461829234461830AG38GENIChomozygous135836249
1234461884234461885CT39GENIChomozygous135836250
1234462300234462301GC50GENIChomozygous135836251
1234462418234462422AAAC42GENIChomozygous145249431
1234462925234462926GA45GENIChomozygous135836255
1234463111234463112AG46GENIChomozygous135836256
1234463144234463145GC43GENIChomozygous135836257
1234463295234463296GA43GENIChomozygous135836258
1234464033234464034CA41GENIChomozygous135836259
1234464196234464197TC55GENIChomozygous135836260
1234464543234464544TA40GENIChomozygous135836261
1234462413234462414AG41GENIChomozygous145336228