chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7108392673108392674GA21GENIChomozygous138177771
7108393849108393850GT17GENIChomozygous138177772
7108394343108394344T8GENIChomozygous137973323
7108396342108396343TC13GENIChomozygous138177776
7108394478108394479GA14GENIChomozygous138177773
7108394606108394607CA16GENIChomozygous138177774
7108394826108394827TC31GENICpossibly homozygous138177775
7108397061108397062GT23GENIChomozygous138177777
7108400973108400974GT23GENIChomozygous138177778
7108402938108402939AT24GENIChomozygous138177779
7108403544108403545CT21GENIChomozygous138177780
7108405289108405290TC13GENIChomozygous138177781
7108405467108405468GA26GENIChomozygous138177782
7108406022108406023AT24GENIChomozygous138177783
7108408800108408801CT33GENIChomozygous138177784
7108408885108408886AG26GENIChomozygous138177785
7108410072108410073GA24GENIChomozygous138177786
7108410142108410143CT28GENIChomozygous138177787
7108410412108410413CT24GENIChomozygous138177788
7108411088108411089CA33GENIChomozygous138177789
7108412104108412105GA17GENIChomozygous138177790
7108412404108412405TC18GENIChomozygous138177791
7108413095108413096GA27GENIChomozygous138177792
7108413366108413367AG27GENIChomozygous138177793
7108400770108400771G14GENICheterozygous403221657
7108400770108400771GT14GENIChomozygous154486268