chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101849180318491804GT26GENICpossibly homozygous130395989
101849296618492967C40GENIChomozygous128792775
101849830418498305G49GENIChomozygous128792777
101849830618498307G49GENIChomozygous128792778
101849831418498315TG45GENIChomozygous116503079
101849838918498390C42GENIChomozygous128792779
101849849218498493G55GENIChomozygous128792780
101849852818498529G55GENIChomozygous128792781
101849853518498535C54GENIChomozygous128792782
101850069318500693G34GENIChomozygous128792785
101850070018500701A32GENIChomozygous128792786
101850070518500706C34GENIChomozygous128792787
101850075118500751T33GENIChomozygous128792788
101850076018500760T31GENIChomozygous128792789
101850077618500776C22GENIChomozygous128792790
101850079218500793CT25GENIChomozygous116861344
101850079318500794TC25GENIChomozygous116861346
101850081018500810G27GENIChomozygous128792791
101850111218501112G2GENIChomozygous130576274
101850112618501127TG2GENIChomozygous117983310
101850127718501278G41GENIChomozygous128792798
101850128218501283AC42GENIChomozygous116918860
101850129618501297C41GENIChomozygous128792799
101850130218501302C43GENIChomozygous128792800
101850133218501332T37GENIChomozygous128792801
101850133918501340GT35GENIChomozygous116918862
101850134618501347C38GENIChomozygous128792802
101850135618501356G38GENIChomozygous128792803
101850135918501360T41GENIChomozygous128792804
101850136918501369A36GENIChomozygous128792805
101850146618501466A45GENIChomozygous128792806
101850147218501473C45GENIChomozygous128792807
101850150018501500G45GENIChomozygous128792808
101850155118501552AT46GENIChomozygous116503085
101850184118501841A41GENIChomozygous128792809
101850184818501849C40GENIChomozygous128792810
101850185618501856C41GENIChomozygous128792811
101850186718501868TG43GENIChomozygous116503099
101850463418504635CG41GENIChomozygous116503121
101850463718504639TG42GENIChomozygous128792813