chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107351346273513462CACACACATGTGCA15GENIChomozygous132146019
107353786173537861A13GENIChomozygous128830433
107355150873551508CAA11GENIChomozygous128830436
107355599873555999CT7GENIChomozygous118001183
107357461473574615CA12GENIChomozygous116800108
107355209473552095GA5GENICheterozygous128871454
107355838873558389AC11GENICheterozygous116800104
107355839573558396AC13GENICheterozygous116800106
107362782573627826AG10GENIChomozygous116635347
107363088773630888AG8GENIChomozygous117064129
107363088973630890AG8GENIChomozygous117064131
107363089673630897CG9GENIChomozygous116635351
107363103673631037GC14GENIChomozygous117016600
107363103973631040AC14GENIChomozygous117016601
107363104073631041AC14GENIChomozygous117016602
107363104273631043AG13GENIChomozygous117064133
107363108373631084CG15GENIChomozygous117016603
107363108873631089C15GENIChomozygous128830475
107363109173631092CA15GENIChomozygous117016604
107363109473631095TG14GENIChomozygous117016605
107363109873631099TG12GENIChomozygous117016606
107363110073631101GC12GENIChomozygous117016607
107363110973631110TC11GENIChomozygous117296436
107363111173631112AC11GENIChomozygous117296438
107363111473631115GC11GENIChomozygous117296440
107363103873631039AC14GENIChomozygous116978925
107361336373613364A29GENICheterozygous131466711