chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X134941028134941029GA3GENIChomozygous108509273
X134944258134944259GA4GENIChomozygous108509279
X134944385134944386AG2GENIChomozygous108509281
X134947652134947653TC5GENIChomozygous108509291
X134947669134947670CG5GENIChomozygous108509293
X134948431134948432AC3GENIChomozygous108509299
X134949895134949896CT3GENIChomozygous108509301
X134950411134950412CT4GENIChomozygous108509303
X134951474134951475TG2GENIChomozygous108509305
X134951986134951987CT2GENIChomozygous108509307
X134952279134952280CT3GENIChomozygous108509309
X134952870134952871CA2GENIChomozygous108509311
X134953503134953504CG5GENIChomozygous108509313
X134955336134955337TC2GENIChomozygous108509315
X134957667134957668CT5GENIChomozygous108530260
X134958326134958327CT3GENIChomozygous108509319
X134958327134958328TC3GENIChomozygous108509321
X134961562134961563CG5GENIChomozygous108509329
X134962348134962349TC2GENIChomozygous108509333
X134962385134962386TA3GENIChomozygous108509335
X134963399134963400CT4GENIChomozygous108509337
X134963658134963659GC4GENIChomozygous108509339
X134964464134964465AC6GENIChomozygous108509343
X134964478134964479AG6GENIChomozygous108509345
X134964533134964534CT3GENIChomozygous108509347
X134965873134965874GA2GENIChomozygous108509353
X134966394134966395CG4GENIChomozygous108509355
X134966478134966479AG2GENIChomozygous108509357
X134966855134966856AG3GENIChomozygous108509359
X134966856134966857GA3GENIChomozygous108509361
X134967034134967035AG4GENIChomozygous108509363
X134967155134967156CA4GENIChomozygous108509365
X134967184134967185CT5GENIChomozygous108509367
X134967478134967479CA3GENIChomozygous108509369
X134967811134967812GA4GENIChomozygous108509371
X134968178134968179AG2GENIChomozygous108509373
X134969031134969032TG3GENIChomozygous108509375
X134969077134969078CT3GENIChomozygous108509377
X134969498134969499GA4GENIChomozygous108509379
X134945542134945543TA4GENIChomozygous108821367
X134945543134945544AC4GENIChomozygous108821368