chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1182525617182525618CT14GENIChomozygous135764538
1182526390182526391GT22GENICpossibly homozygous135764539
1182528039182528045AGAACC7GENIChomozygous135449357
1182528078182528086AAATAAAA7GENIChomozygous135449358
1182529200182529201TG14GENIChomozygous135764540
1182529487182529488T13GENIChomozygous135449359
1182529619182529620GA10GENIChomozygous135764541
1182530179182530180GT14GENIChomozygous135764542
1182530477182530478AG14GENIChomozygous135764543
1182533251182533252GA13GENIChomozygous135764544
1182535167182535168GT19GENIChomozygous135764545
1182532167182532183AAGAAAGGAGGGAAAG19GENIChomozygous135449360