chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101849180318491804GT5GENIChomozygous130395989
101849296618492967C21GENIChomozygous128792775
101849830418498305G20GENIChomozygous128792777
101849830618498307G20GENIChomozygous128792778
101849831418498315TG20GENIChomozygous116503079
101849838918498390C18GENIChomozygous128792779
101849849218498493G20GENIChomozygous128792780
101849852818498529G15GENIChomozygous128792781
101849853518498535C14GENIChomozygous128792782
101850069318500693G3GENIChomozygous128792785
101850070018500701A5GENIChomozygous128792786
101850070518500706C5GENIChomozygous128792787
101850075118500751T5GENIChomozygous128792788
101850076018500760T5GENIChomozygous128792789
101850077618500776C8GENIChomozygous128792790
101850079218500793CT9GENIChomozygous116861344
101850079318500794TC9GENIChomozygous116861346
101850081018500810G11GENIChomozygous128792791
101850084818500848G14GENIChomozygous128792792
101850085818500858G16GENIChomozygous128792793
101850088018500880G15GENIChomozygous128792794
101850088418500884T15GENIChomozygous128792795
101850091518500915G13GENIChomozygous128792796
101850130218501302C11GENIChomozygous128792800
101850133218501332T7GENIChomozygous128792801
101850133918501340GT7GENIChomozygous116918862
101850134618501347C8GENIChomozygous128792802
101850135618501356G8GENIChomozygous128792803
101850135918501360T10GENIChomozygous128792804
101850136918501369A11GENIChomozygous128792805
101850146618501466A15GENIChomozygous128792806
101850147218501473C15GENIChomozygous128792807
101850150018501500G15GENIChomozygous128792808
101850155118501552AT15GENIChomozygous116503085
101850184118501841A17GENIChomozygous128792809
101850184818501849C16GENIChomozygous128792810
101850185618501856C19GENIChomozygous128792811
101850186718501868TG19GENIChomozygous116503099
101850463418504635CG17GENIChomozygous116503121
101850463718504639TG16GENIChomozygous128792813