chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
78356462683564627CT31GENICheterozygous803471414
78356464383564644TA33GENICheterozygous803471415
78356571683565717AT14GENIChomozygous803471416
78356593483565935AG22GENIChomozygous803471417
78356603683566037TC22GENIChomozygous803471418
78356714483567145TC9GENIChomozygous803471419
78356820283568203CT24GENIChomozygous803471420
78356874483568745AG20GENIChomozygous803471421
78356909183569092GA24GENIChomozygous803471422
78356927283569273AG10GENIChomozygous803471423
78357005383570054TG13GENIChomozygous803471424
78357084983570850CT7GENIChomozygous803471425
78357093983570940CT14GENIChomozygous803471426
78357154283571543TG18GENIChomozygous803471427
78357207483572075CT21GENIChomozygous803471428
78357241383572414GC20GENIChomozygous803471429
78357313583573136CA23GENICpossibly homozygous803471430
78357557383575574TC8GENIChomozygous803471431
78357592183575922GA12GENIChomozygous803471432
78357616983576170TG11GENIChomozygous803471433
78357676283576763AG25GENIChomozygous803471434
78357902083579021TC21GENIChomozygous803471435
78358005483580055AG15GENIChomozygous803471436
78358114783581148GA27GENIChomozygous803471437
78358150483581505GA41GENIChomozygous803471438
78358156183581562TG25GENIChomozygous803471439
78358222983582230GT26GENIChomozygous803471440