chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1250200520250200521CT16INTERGENIChomozygous75885704
1250201108250201109CA17INTERGENICheterozygous75276173
1250202053250202054CT16INTERGENIChomozygous75276179
1250204861250204862CA19INTERGENIChomozygous74815980
1250204998250204999AC24INTERGENIChomozygous75276187
1250206564250206565TC9INTERGENIChomozygous74815986
1250206576250206577TC13INTERGENIChomozygous74815989
1250206828250206829TC16INTERGENIChomozygous75747322
1250202966250202967CT20INTERGENIChomozygous75747318
1250203977250203978CT19INTERGENIChomozygous75747319
1250204367250204368TC14INTERGENIChomozygous75747320
1250206008250206009GT15INTERGENIChomozygous75747321
1250219564250219565GC16INTERGENICheterozygous74816043
1250223838250223839TC23INTERGENIChomozygous74816057
1250227215250227216GA19INTERGENIChomozygous75747323
1250385123250385124AG18INTERGENIChomozygous74816098
1250407807250407808AG17INTERGENIChomozygous74816110
1250409754250409755GT11INTERGENIChomozygous76478945
1250410343250410344TC19INTERGENIChomozygous74816113
1250410752250410753CT27INTERGENIChomozygous75276314
1250410966250410967AG23INTERGENIChomozygous75276316
1250411122250411123GT19INTERGENIChomozygous76478946
1250411250250411251CT16INTERGENIChomozygous75276318
1250412296250412297CA11INTERGENIChomozygous75276322
1250412420250412421GA12INTERGENICheterozygous76396065
1250412616250412617GA14INTERGENIChomozygous75276324
1250413116250413117CT13INTERGENIChomozygous75276326
1250413776250413777AG16INTERGENIChomozygous75276328
1250413831250413832CT5INTERGENICheterozygous75276330
1250414438250414439AT30INTERGENIChomozygous75276334
1250414686250414687GA20INTERGENIChomozygous75276336
1250415294250415295TC28INTERGENIChomozygous74816128
1250415308250415309AC27INTERGENIChomozygous74816131
1250415844250415845TG17INTERGENIChomozygous74816137
1250416392250416393CT18INTERGENIChomozygous76670393
1250416610250416611TC20INTERGENIChomozygous74816140
1250416760250416761GT28INTERGENIChomozygous74816143