chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7115318660115318661TC20GENIChomozygous138187279
7115318780115318781GA21GENIChomozygous142008920
7115318930115318931GT21GENIChomozygous138187280
7115320471115320472GT19GENIChomozygous138187286
7115322208115322208GGAG14GENIChomozygous137975862
7115322297115322298CT9GENIChomozygous142008921
7115324090115324091GC13GENIChomozygous142008922
7115325829115325830GC24GENIChomozygous142008923
7115325838115325839AG25GENIChomozygous138187290
7115325840115325840G25GENIChomozygous141922839
7115325844115325845AG27GENIChomozygous138187291
7115327455115327456AG19GENIChomozygous138187293
7115327775115327776CT23GENIChomozygous142008924
7115328247115328248CT19GENIChomozygous142008925
7115328512115328513TC12GENIChomozygous138187294
7115329725115329725C18GENIChomozygous137975864
7115332157115332158GA34GENIChomozygous142008926
7115333388115333389GA19GENIChomozygous142008927
7115333602115333603GA16GENIChomozygous142008928
7115335224115335225TC18GENIChomozygous138187313
7115335997115335998AT18GENIChomozygous142008929
7115336080115336080GT6GENIChomozygous141922840
7115336655115336655TG8GENIChomozygous137975868
7115337589115337590GC20GENIChomozygous138187318
7115337615115337616TA22GENIChomozygous142008930
7115339385115339386TC21GENIChomozygous138187324
7115341191115341192TG18GENIChomozygous138187326
7115322404115322405A7GENICheterozygous403223172
7115322404115322405AG7GENIChomozygous154480457