chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X118445539118445540TC22GENIChomozygous108316156
X118447932118447933CT11GENIChomozygous108316158
X118447933118447934TG11GENIChomozygous108316160
X118448630118448631GA27GENIChomozygous108316162
X118452010118452011GA26GENIChomozygous108316164
X118452626118452627GA17GENIChomozygous108316166
X118452880118452881GC16GENIChomozygous108316168
X118456045118456046CT21GENIChomozygous108316170
X118457608118457609CT20GENIChomozygous108454165
X118462153118462154TA6GENIChomozygous108316172
X118467279118467280AG14GENIChomozygous108316174
X118469922118469923GA23GENIChomozygous108316176
X118472970118472971GA19GENIChomozygous108316178
X118473328118473329AG19GENIChomozygous108419830
X118475134118475135TA17GENIChomozygous108419832
X118483734118483735TG15GENIChomozygous108316180
X118492842118492843AG19GENIChomozygous108316182
X118493383118493384GC20GENIChomozygous108316184
X118495775118495776CT30GENIChomozygous108316186
X118503022118503023CT23GENIChomozygous108316188
X118503074118503075CT31GENIChomozygous108316190
X118503647118503648GA22GENIChomozygous108316192
X118504183118504184GC18GENIChomozygous108316196
X118504333118504334CT22GENIChomozygous108316198
X118504354118504355CA19GENIChomozygous108316200
X118504356118504357GA20GENIChomozygous108316202
X118505392118505393GA17GENIChomozygous108316204
X118508081118508082CG19GENIChomozygous108316206
X118508088118508089TA20GENIChomozygous108316208
X118508401118508402GA22GENIChomozygous108316210
X118511529118511530AG22GENIChomozygous108316212
X118513958118513959TC21GENIChomozygous108316214
X118514352118514353AG12GENIChomozygous108419834