chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5153691433153691434GA7GENIChomozygous137655326
5153691490153691491GA8GENIChomozygous137655327
5153693371153693371G6GENIChomozygous137350157
5153693375153693376AG6GENIChomozygous137655328
5153696583153696584TC18GENIChomozygous137655329
5153697346153697347TC11GENIChomozygous137655330
5153698015153698016TC9GENIChomozygous137655331
5153698275153698275TG8GENIChomozygous137350158
5153698292153698293TC9GENIChomozygous137655332
5153699622153699623CT17GENIChomozygous137655333
5153699815153699816AG17GENIChomozygous137655334
5153700091153700092CT15GENIChomozygous137655335
5153700092153700093CA15GENIChomozygous137655336
5153700111153700112AG16GENIChomozygous137655337
5153700620153700621AC16GENIChomozygous137655338
5153701191153701192AT5GENICheterozygous154262840
5153701191153701192A5GENIChomozygous403163489
5153703867153703868AC4GENIChomozygous137655339
5153704283153704284GT14GENIChomozygous137655340
5153704444153704445GA13GENIChomozygous137655341
5153704632153704633CT16GENIChomozygous137655342
5153705275153705276AC15GENIChomozygous137655343
5153705641153705642CA14GENIChomozygous137655344
5153705645153705646TA16GENIChomozygous137655345
5153705650153705651GA18GENIChomozygous137655346
5153705651153705652CT18GENIChomozygous137655347
5153705655153705656CT16GENIChomozygous137655348
5153705693153705694CT16GENIChomozygous137655349