chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153137496131374962AG169GENICheterozygous48272523
153137498831374989CA191GENICheterozygous48579810
153137503631375037CT194GENICheterozygous48272524
153137522931375230AG90GENICheterozygous48272526
153137524931375250TG83GENICheterozygous48817186
153137525031375251GA85GENICheterozygous49495039
153137525631375257CT90GENICheterozygous48272527
153137531131375312AG95GENICheterozygous48272528
153137531631375317TC96GENICheterozygous48272529
153137533631375337CT94GENICheterozygous48272530
153137537531375376AG106GENICheterozygous48272531
153137538931375390AC108GENICheterozygous48272532
153137543331375434AT102GENICheterozygous48272533
153137544131375442TC106GENICheterozygous48272534
153137545031375451CT107GENICheterozygous48272535
153137558031375581GA90GENICheterozygous48272538
153137559731375598TC91GENICheterozygous48272539
153137561231375613AC91GENICheterozygous48272540
153137563131375632GA88GENICheterozygous48272541
153137570331375704AG99GENICheterozygous48579812
153137574031375741TG78GENICheterozygous48272542