chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107355599873555999CT22GENICpossibly homozygous118001183
107355838873558389AC92GENICheterozygous116800104
107355839573558396AC87GENICheterozygous116800106
107357461473574615CA31GENICpossibly homozygous116800108
107359945973599460AG36GENICheterozygous118068359
107362420673624207AC52GENICheterozygous117391677
107362427473624275CT91GENICheterozygous117197174
107362430873624309AT98GENICheterozygous117197176
107362432673624327GC106GENICheterozygous117142758
107362434473624345AT122GENICheterozygous116635341
107362438673624387CG103GENICheterozygous116635343
107362782573627826AG28GENIChomozygous116635347
107363088773630888AG14GENIChomozygous117064129
107363088973630890AG13GENIChomozygous117064131
107363089673630897CG14GENIChomozygous116635351
107363108373631084CG11GENIChomozygous117016603
107363109173631092CA9GENIChomozygous117016604
107363109473631095TG9GENIChomozygous117016605
107363109873631099TG9GENIChomozygous117016606
107363110073631101GC9GENIChomozygous117016607
107363110973631110TC9GENIChomozygous117296436
107363111173631112AC9GENIChomozygous117296438
107363111473631115GC10GENIChomozygous117296440