chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76178560361785604GA42GENIChomozygous115690454
76178609561786096TC10GENIChomozygous115690455
76178906061789061CA13GENICheterozygous116179896
76178948061789481AG37GENIChomozygous115690457
76179085161790852GT26GENIChomozygous116333365
76179213561792136AT40GENIChomozygous116333366
76179364661793647TG15GENIChomozygous115690459
76179371761793718CT16GENIChomozygous116333367
76179429261794293TC9GENIChomozygous115690460
76179443761794438AG39GENIChomozygous115690461
76179608561796086AG26GENIChomozygous116333368
76179769161797692AG34GENIChomozygous115690465
76180041161800412GA30GENIChomozygous115690468
76180075761800758GA33GENIChomozygous115690469
76180131561801316AG22GENIChomozygous116333369
76180213161802132AT60GENICheterozygous116333370
76180213361802134TA61GENICpossibly homozygous116333371
76180274661802747TC31GENIChomozygous115690474
76180276661802767AG33GENIChomozygous116333372
76180380761803808TC37GENIChomozygous115690478
76180499961805000TC38GENIChomozygous115690481
76180518361805184TA28GENIChomozygous115690482
76180668461806685AC19GENIChomozygous116333374
76180680461806805AG27GENIChomozygous115690486
76180743361807434TC6GENIChomozygous115690487
76181112061811121GA73GENICheterozygous116406987
76180197161801972TA25GENICheterozygous116406984
76180197761801978TA29GENICheterozygous116406985
76180198961801990TA29GENICheterozygous116406986
76181296561812966CG26GENIChomozygous115690494
76181325561813256CG22GENIChomozygous116333377
76181546461815465AG8GENIChomozygous115690500
76181583061815831CT21GENIChomozygous116333378