chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7115318660115318661TC46GENIChomozygous138187279
7115318780115318781GA65GENIChomozygous142008920
7115318930115318931GT52GENIChomozygous138187280
7115320471115320472GT53GENIChomozygous138187286
7115322208115322208GGAG31GENIChomozygous137975862
7115322297115322298CT38GENIChomozygous142008921
7115324090115324091GC50GENIChomozygous142008922
7115325829115325830GC54GENIChomozygous142008923
7115325838115325839AG54GENIChomozygous138187290
7115325844115325845AG53GENIChomozygous138187291
7115327455115327456AG56GENIChomozygous138187293
7115327775115327776CT59GENIChomozygous142008924
7115328247115328248CT58GENIChomozygous142008925
7115328512115328513TC59GENIChomozygous138187294
7115329725115329725C41GENIChomozygous137975864
7115332157115332158GA62GENIChomozygous142008926
7115333388115333389GA43GENIChomozygous142008927
7115333602115333603GA45GENIChomozygous142008928
7115335224115335225TC56GENIChomozygous138187313
7115335997115335998AT39GENIChomozygous142008929
7115336655115336655TG32GENIChomozygous137975868
7115337589115337590GC60GENIChomozygous138187318
7115337615115337616TA56GENIChomozygous142008930
7115339385115339386TC51GENIChomozygous138187324
7115341191115341192TG58GENIChomozygous138187326
7115325840115325840G54GENIChomozygous141922839
7115322404115322405AG23GENICpossibly homozygous154480457
7115336080115336080GT11GENICheterozygous141922840
7115322404115322405A23GENICheterozygous403223172