chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141326137141326138TG11GENIChomozygous108260455
1141326880141326881GA21GENIChomozygous108260457
1141329766141329767CG3GENICheterozygous108260463
1141331410141331411TC9GENIChomozygous108260465
1141333886141333887AG24GENIChomozygous108260467
1141334815141334816TC22GENIChomozygous108260469
1141335886141335887CT21GENIChomozygous108260471
1141336689141336690AC21GENIChomozygous108260473
1141337526141337527GA10GENIChomozygous108260475
1141337885141337886CT17GENIChomozygous108260477
1141338089141338090GA8GENIChomozygous108260479
1141341241141341242AC20GENIChomozygous108260483
1141341849141341850TA13GENIChomozygous108260485
1141341879141341880CA17GENIChomozygous108260487
1141342026141342027GA17GENIChomozygous108260489
1141342238141342239AG10GENIChomozygous108260491
1141343004141343005CT11GENIChomozygous108260497
1141343452141343453TC21GENIChomozygous108260499
1141344705141344706CT21GENIChomozygous108260501
1141347341141347342TC11GENIChomozygous108260503
1141347743141347744AT18GENIChomozygous108260505
1141348005141348006AT21GENIChomozygous108260507
1141348173141348174TG14GENIChomozygous108260509
1141348515141348516AG12GENIChomozygous108260511
1141349272141349273CT19GENIChomozygous108260513
1141349293141349294GA19GENIChomozygous108260515