chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117744886177448862AG16GENIChomozygous50893275
117744941377449414GC23GENIChomozygous51224798
117744954877449549TC30GENIChomozygous50893277
117744995577449956TC21GENIChomozygous51590516
117745032777450328TC16GENIChomozygous51224801
117745084277450843GA25GENIChomozygous51224805
117745096077450961AG21GENIChomozygous50893279
117745151177451512GA15GENIChomozygous51224807
117745173277451733TC21GENIChomozygous51224809
117745183477451835TC24GENIChomozygous50893287
117745223677452237CT17GENIChomozygous51224811
117745238777452388TC20GENIChomozygous51224813
117745243277452433GA17GENIChomozygous51224815
117745259077452591TC22GENIChomozygous51224817
117745260977452610GC22GENIChomozygous51224819
117745296277452963T-17GENIChomozygous50893293
117745301377453014CG31GENIChomozygous51224823
117745320777453210AAA---18GENIChomozygous51590518
117745321077453211AT18GENIChomozygous51590520
117745349777453498GA32GENIChomozygous51224825
117745372077453721TC22GENIChomozygous51224829
117745390077453903AAA---10GENIChomozygous50893301
117745396477453965TTAGCA14GENIChomozygous50893303
117745396877453969T-15GENIChomozygous50893305
117745396577453966TA14GENIChomozygous51190049
117745399077453996TGTGTG------3GENIChomozygous51190051
117745520577455206AG20GENIChomozygous50893307
117745521677455217CT18GENIChomozygous51590521
117745549577455496CCTCT14GENIChomozygous50893311
117745552377455524TC15GENIChomozygous51590523
117745553477455535T-12GENIChomozygous50893313
117745585877455859AG19GENIChomozygous50893315
117745585977455860AC20GENIChomozygous50893317
117745634677456347AG17GENIChomozygous50893319
117745654177456542GA16GENIChomozygous50893321
117745655277456553GA20GENIChomozygous50893323