chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X124723280124723281TC6GENIChomozygous108326267
X124725082124725083AG10GENIChomozygous108326273
X124725898124725899CG13GENIChomozygous108424725
X124726205124726206GA7GENIChomozygous108326275
X124731973124731974AC11GENIChomozygous108326277
X124734856124734857CT11GENIChomozygous108326279
X124741491124741492TC11GENIChomozygous108326281
X124742681124742682AG5GENIChomozygous108424727
X124743427124743428AC11GENICpossibly homozygous108326283
X124743935124743936AG9GENIChomozygous108326285
X124728537124728538A10GENIChomozygous129787176
X124744963124744964CG7GENIChomozygous108811714
X124745634124745635TC10GENIChomozygous108326289
X124746866124746867CT10GENIChomozygous108326291
X124747331124747332GA8GENIChomozygous108326293
X124748552124748553TA16GENIChomozygous108326295
X124749078124749079GA17GENIChomozygous108326297
X124749205124749205ACCTGATGTCA9GENIChomozygous129787177
X124750926124750926A11GENIChomozygous129787178
X124750979124750979T12GENIChomozygous129787179
X124751241124751245CACT9GENIChomozygous129787180
X124751246124751248AC10GENIChomozygous129787181
X124751249124751250GC10GENIChomozygous108326303
X124753199124753200GA14GENIChomozygous108326305
X124753405124753406CT12GENIChomozygous108326307
X124754472124754473A8GENICpossibly homozygous129787182
X124757222124757223TG13GENIChomozygous108326309
X124757735124757736AG12GENIChomozygous108326311
X124759581124759582CT13GENIChomozygous108326313
X124759853124759854CT7GENIChomozygous108326315
X124760647124760648TA6GENIChomozygous108326317
X124761379124761380GA3GENIChomozygous108326319
X124756799124756800AG6GENIChomozygous108635320