chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35965361659653617TC5GENIChomozygous112125885
35965491759654918T5GENICheterozygous127887448
35965604259656043CA12GENIChomozygous112125886
35966090559660905A16GENIChomozygous127887449
35966387559663877CA23GENIChomozygous127887450
35966753059667531CA19GENIChomozygous111583947
35966752959667530AG19GENIChomozygous111911038
35966798259667983TA26GENIChomozygous111583948
35966565559665656CG17GENIChomozygous111583944
35966653359666534CT17GENIChomozygous111583945
35966749359667494TC20GENIChomozygous111583946
35966941659669417AG20GENIChomozygous111583949
35967210659672107GA10GENIChomozygous111583950
35967691759676918AG19GENIChomozygous111583951
35967744459677444A20GENIChomozygous127887451
35967910059679101CT37GENIChomozygous111583952
35968034259680343CT23GENIChomozygous111583953
35968206259682063AT26GENIChomozygous111583954
35968270359682704AT12GENIChomozygous111583955
35968334059683341AG18GENIChomozygous111583956
35968362159683622TA20GENIChomozygous111583957
35968385459683855GA30GENIChomozygous111583958
35968392959683930GA27GENIChomozygous111583959
35968492459684925TC19GENIChomozygous111583960
35968565259685653CT27GENIChomozygous111583961
35968607659686077TG20GENIChomozygous111583962
35968608859686089TG22GENIChomozygous111583963
35968484659684847GT22GENIChomozygous119649580
35967758259677588TATATA19GENIChomozygous127887452
35968312159683121AT18GENIChomozygous127887453
35968484559684846C22GENIChomozygous127887454
35968493059684934TTAC20GENIChomozygous127887455
35968610059686100TCCCCGTGGG23GENIChomozygous127887456
35968678659686786AACTTT11GENIChomozygous127887457
35968675459686755GA18GENIChomozygous111583964