chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104815361248153617GGGTG38GENIChomozygous133228401
104815374948153750AT16GENIChomozygous117129101
104815376348153764TC17GENIChomozygous117059173
104815422448154225A45GENIChomozygous128815084
104815423248154234GG45GENIChomozygous128815085
104815424548154246A42GENIChomozygous128815086
104815425048154251AG42GENIChomozygous116588434
104815434548154345G30GENIChomozygous128815087
104815437648154376T26GENIChomozygous128815088
104816420748164208CT71GENIChomozygous116588456
104816708648167087AG61GENIChomozygous116588458
104816738048167381AT46GENIChomozygous116588460
104817365548173655TTTGT66GENIChomozygous128815096
104817451748174518TC51GENIChomozygous116588468
104818421548184219ATAC41GENIChomozygous133228402
104818668348186684A47GENIChomozygous128815101
104818681748186818GA67GENICpossibly homozygous117009035
104816625548166256GA56GENIChomozygous117009033
104817560348175604GA45GENIChomozygous117009034
104817123448171235TG23GENIChomozygous116931961
104817139848171399GC4GENIChomozygous133236694
104817141248171413T4GENIChomozygous130392299
104819121148191212TG42GENIChomozygous133236695
104819332548193326TC67GENIChomozygous116588486
104819377048193771GT54GENIChomozygous116588488
104820311348203114CA13GENIChomozygous117993733
104820394748203949TG14GENIChomozygous128815110
104820398648203986G10GENIChomozygous128815111
104820638448206387TGT2GENIChomozygous132691732
104820639548206395T5GENIChomozygous130392303
104820775748207758T64GENIChomozygous133228403
104820978848209789C51GENIChomozygous133228404