chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X8264955582649556GA17GENICheterozygous120086137
X8265497482654975TG6GENIChomozygous108280370
X8266048982660490AT13GENIChomozygous108280372
X8266701582667016GA12GENIChomozygous108280374
X8267133582671336GA4GENIChomozygous108280376
X8267308982673090AG8GENICpossibly homozygous108280378
X8267518982675190GA4GENICheterozygous120086139
X8267896082678961CT3GENIChomozygous108280380
X8269431082694311GA6GENICheterozygous119930774
X8270102282701023TC7GENIChomozygous108280382
X8270229982702300TA40GENICheterozygous119930775
X8270238782702388CT73GENICheterozygous119930776
X8270304682703047GT6GENICheterozygous120086141
X8270319182703192GA26GENICheterozygous120086143
X8270383882703839AT19GENICheterozygous119930781
X8270384382703844TA19GENICheterozygous119930782
X8270769782707698CT5GENIChomozygous108280384
X8271321382713214GA6GENIChomozygous120086145
X8271630482716305GC9GENIChomozygous108280386
X8272395482723955TG4GENIChomozygous108280388
X8270067682700677TC9GENIChomozygous108396573
X8271483682714837AG4GENICheterozygous108396575
X8270227882702279AG26GENICheterozygous120070401
X8272927382729274CA3GENIChomozygous108280392
X8273851082738511TA5GENIChomozygous108280396
X8274365382743654TC13GENIChomozygous108280398