chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
65673463356734634TC55GENIChomozygous114809207
65673981556739816GA18GENIChomozygous114809212
65674013356740134CT15GENIChomozygous114809213
65674037856740379TG12GENIChomozygous114809215
65674493856744939AT22GENIChomozygous114809219
65674719856747199AC22GENIChomozygous114809234
65674728556747286TG21GENIChomozygous114809235
65674814856748149AT23GENIChomozygous114809238
65674865356748654AG33GENIChomozygous114809240
65675011056750111AG30GENICpossibly homozygous114809243
65675084856750849GA21GENIChomozygous114809247
65675571456755715AG26GENIChomozygous114809262
65675748756757488CA20GENIChomozygous114809264
65675847556758476CT29GENIChomozygous114809266
65675848256758483TC27GENIChomozygous114809267
65676144356761444AG23GENIChomozygous114809269
65676316956763170CT18GENIChomozygous114809271
65676550556765506AG28GENIChomozygous114809273
65676571456765715CG38GENIChomozygous114809274
65676578756765788AG42GENIChomozygous114809276
65676620956766210TC18GENIChomozygous114809278
65676809556768096TC25GENIChomozygous114809280
65677054956770550AG35GENIChomozygous114809281
65677071356770714GA36GENIChomozygous114809283
65677089356770894TC31GENIChomozygous114809285
65677142256771423CA28GENIChomozygous114809287
65677199056771991CT10GENIChomozygous114809288
65677260356772604TC27GENIChomozygous114809290
65677468456774685AG21GENIChomozygous114809293