chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2115167990115167991CT17GENIChomozygous820977799
2115170589115170590TC14GENIChomozygous820977800
2115172510115172511GT15GENIChomozygous820977801
2115173033115173035AA--10GENICheterozygous820977802
2115173035115173037AC--10GENICheterozygous820977803
2115173042115173043CA8GENICheterozygous820977804
2115173049115173051AA--8GENICheterozygous820977805
2115174000115174001GGT15GENIChomozygous820977806
2115176746115176747AG13GENIChomozygous820977807
2115179250115179251AC17GENIChomozygous820977808
2115180915115180916GA13GENIChomozygous820977809
2115181419115181423TGTT----12GENIChomozygous820977810
2115181754115181755T-10GENIChomozygous820977811
2115182303115182304AAG8GENIChomozygous820977812
2115185464115185465GT13GENIChomozygous820977813
2115188696115188697CT24GENIChomozygous820977814
2115189610115189611TTG12GENIChomozygous820977815
2115203046115203047CT18GENIChomozygous820977816
2115203268115203269GC11GENIChomozygous820977817
2115203550115203551GA8GENIChomozygous820977818
2115204116115204117CG17GENIChomozygous820977819
2115204122115204123TTG17GENIChomozygous820977820
2115204469115204470CA8GENIChomozygous820977821
2115204494115204496TA--11GENIChomozygous820977822
2115204986115204987CT7GENIChomozygous820977823
2115204996115204997CT7GENIChomozygous820977824
2115205049115205050AC10GENIChomozygous820977825
2115205802115205803GA13GENIChomozygous820977826
2115206087115206088AG15GENIChomozygous820977827
2115206214115206215AC16GENIChomozygous820977828
2115206219115206220AT16GENIChomozygous820977829
2115207147115207148C-17GENIChomozygous820977830
2115209178115209180TT--8GENIChomozygous820977831
2115210346115210347CT16GENIChomozygous820977832
2115210788115210789GGTT20GENICpossibly homozygous820977833
2115211304115211305CT18GENIChomozygous820977834
2115212843115212846TGG---13GENIChomozygous820977835
2115214710115214711CT12GENIChomozygous820977836