chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1250580074250580074G18GENIChomozygous127503233
1250580086250580086A21GENIChomozygous127503234
1250580102250580103G23GENIChomozygous127503235
1250580112250580113T23GENIChomozygous127503236
1250580145250580145C27GENIChomozygous127503237
1250580168250580169T25GENIChomozygous127503238
1250580176250580177TA22GENIChomozygous120493910
1250580177250580178AT22GENIChomozygous120476873
1250580187250580188A21GENIChomozygous127503239
1250580234250580235C13GENIChomozygous127503240
1250596585250596586TC17GENICheterozygous130241513
1250596814250596815TA13GENICheterozygous130241514
1250597042250597043TC23GENICheterozygous108608241
1250597088250597089CT16GENICheterozygous108778164
1250597101250597102GC13GENICheterozygous109544516
1250597130250597131GA13GENICheterozygous130241515
1250597169250597170CT12GENICheterozygous130241516
1250601761250601762CA49GENIChomozygous108608250
1250616203250616204C3GENIChomozygous127503249
1250620509250620510G4GENIChomozygous130218140
1250620494250620496TG6GENIChomozygous130218137
1250620500250620500C5GENIChomozygous130218138
1250620505250620506G4GENIChomozygous130218139
1250620519250620520A4GENIChomozygous130218141
1250620523250620523C4GENIChomozygous130218142
1250620529250620530G5GENIChomozygous130218143
1250620531250620532T5GENIChomozygous130218144
1250620537250620538A6GENIChomozygous130218145
1250620541250620541C6GENIChomozygous130218146
1250620557250620557CCTCCCC4GENIChomozygous130218147
1250620562250620563T9GENIChomozygous130218148
1250620567250620568TC10GENIChomozygous109544518
1250656699250656700AC43GENIChomozygous108608412