chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214375955214375956TC12GENIChomozygous108532379
1214376175214376175CTT14GENIChomozygous127481169
1214376451214376452A13GENIChomozygous127481170
1214376726214376728CC18GENICheterozygous127481171
1214377125214377126T18GENIChomozygous127481172
1214377502214377503TC19GENIChomozygous108532380
1214377599214377600CA21GENIChomozygous108532381
1214377709214377710TG21GENIChomozygous108532382
1214377935214377936CA19GENIChomozygous108532383
1214378023214378025AC20GENIChomozygous127481173
1214378309214378310CT21GENIChomozygous108532384
1214378393214378394CA18GENIChomozygous121174421
1214378464214378465CT23GENIChomozygous108532385
1214378647214378648GA27GENIChomozygous108532386
1214379430214379431AG19GENIChomozygous108532387
1214379707214379708GC17GENIChomozygous108532388
1214379953214379954AG13GENIChomozygous108532389
1214380033214380034CG14GENIChomozygous108532390
1214380178214380179AG9GENIChomozygous108532391
1214381179214381180CT20GENIChomozygous108532392
1214381761214381762CT10GENIChomozygous108532393
1214381939214381940GT1GENIChomozygous108532394
1214382436214382437GA30GENIChomozygous108532398
1214382582214382583AC21GENIChomozygous108532399
1214382788214382789TC26GENIChomozygous108532400
1214384631214384632GA24GENIChomozygous108532401