chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5153691433153691434GA51GENIChomozygous137655326
5153691490153691491GA52GENIChomozygous137655327
5153693375153693376AG20GENIChomozygous137655328
5153693371153693371G20GENIChomozygous137350157
5153696583153696584TC59GENIChomozygous137655329
5153697346153697347TC63GENIChomozygous137655330
5153698015153698016TC52GENIChomozygous137655331
5153698275153698275TG32GENIChomozygous137350158
5153698292153698293TC38GENIChomozygous137655332
5153699622153699623CT54GENIChomozygous137655333
5153699815153699816AG49GENIChomozygous137655334
5153700091153700092CT44GENIChomozygous137655335
5153700092153700093CA43GENIChomozygous137655336
5153700111153700112AG46GENIChomozygous137655337
5153700620153700621AC41GENIChomozygous137655338
5153703867153703868AC9GENIChomozygous137655339
5153704283153704284GT47GENIChomozygous137655340
5153704444153704445GA61GENIChomozygous137655341
5153704632153704633CT65GENIChomozygous137655342
5153705275153705276AC69GENIChomozygous137655343
5153705641153705642CA56GENIChomozygous137655344
5153705645153705646TA58GENIChomozygous137655345
5153705650153705651GA59GENIChomozygous137655346
5153705651153705652CT59GENIChomozygous137655347
5153705655153705656CT58GENIChomozygous137655348
5153705693153705694CT65GENIChomozygous137655349
5153701191153701192A17GENIChomozygous403163489
5153701191153701192AT17GENICheterozygous154262840