chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151294921812949219GA3GENICheterozygous125783780
151300029513000296TA8GENIChomozygous125771078
151300029813000299AG6GENIChomozygous125771079
151300030813000309CT8GENIChomozygous125771080
151300035313000354AG5GENIChomozygous125771081
151301054413010545AG15GENIChomozygous125771083
151301063913010640TA7GENIChomozygous125771084
151301071213010713TA12GENIChomozygous125771085
151305366913053670GC4GENICheterozygous125783781
151309148913091490CG7GENIChomozygous125771092
151312818113128182CA8GENIChomozygous125783782
151312823113128232GC17GENIChomozygous125771094
151313614013136141AG4GENIChomozygous125771096
151318490613184907CT3GENICheterozygous125783783
151332165313321654GA4GENIChomozygous112453756
151332186313321864CA4GENIChomozygous112453757
151334286513342866AT6GENIChomozygous125771103
151334290713342908GC5GENIChomozygous125783784
151334682813346829CA10GENIChomozygous125771105
151334688613346887AC17GENIChomozygous125771106
151336893513368936GA11GENIChomozygous113194642
151336895313368954TC9GENIChomozygous112985235
151336897413368975GA5GENIChomozygous118870639
151336897913368980GC5GENIChomozygous118870641
151336898413368985TC4GENIChomozygous125783785
151336902613369027TA16GENIChomozygous118870645
151339043313390434AG16GENIChomozygous125771108
151339067213390673GT8GENIChomozygous112453932
151339070713390708TC17GENIChomozygous125771110
151339081113390812CA11GENIChomozygous125771111
151339083313390834CT11GENIChomozygous125771112
151359028913590290GT3GENICheterozygous125783786
151362976513629766GT4GENICheterozygous125783787