chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6118006815118006816AG22GENIChomozygous55263860
6118006821118006822AATGTGTGTG18GENIChomozygous55532883
6118006862118006868GTGTGT------5GENIChomozygous55050776
6118006966118006967TC23GENIChomozygous55263865
6118007202118007203CT9GENIChomozygous55263867
6118007288118007289GA10GENIChomozygous55263870
6118007317118007318AAGGGCTGG6GENICheterozygous55532885
6118007320118007321AATTTAGCTCAGTGGTAGAGCGCTTACCT6GENICheterozygous55532887
6118007350118007351AAACACACAC5GENIChomozygous54960002
6118007433118007444AAATAAAACTT-----------6GENIChomozygous55263873
6118008292118008293TA38GENIChomozygous55263875
6118008916118008917GGC19GENIChomozygous55263878
6118008918118008926TGGTTGTG--------24GENIChomozygous55263880
6118008927118008928GC21GENIChomozygous55532889
6118008929118008930CCATT20GENIChomozygous55263883
6118009040118009042CC--15GENIChomozygous55263885
6118009751118009752GGA13GENIChomozygous55263888
6118009759118009760CA15GENIChomozygous55263890
6118010166118010167GT28GENIChomozygous55263892
6118010236118010237CT21GENIChomozygous55263895
6118011842118011843CT21GENIChomozygous55263897
6118012262118012263GT8GENIChomozygous55263900
6118012275118012276CG8GENIChomozygous55263902
6118012296118012297AG6GENIChomozygous55263905
6118012537118012538CT14GENIChomozygous55263907