chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6118006815118006816AG13GENIChomozygous55263860
6118006821118006822AATGTGTGTG11GENIChomozygous55532883
6118006862118006868GTGTGT------4GENICheterozygous55050776
6118006966118006967TC10GENIChomozygous55263865
6118007202118007203CT9GENIChomozygous55263867
6118007288118007289GA15GENIChomozygous55263870
6118007317118007318AAGGGCTGG10GENICheterozygous55532885
6118007320118007321AATTTAGCTCAGTGGTAGAGCGCTTACCT10GENICheterozygous55532887
6118007433118007444AAATAAAACTT-----------11GENIChomozygous55263873
6118008292118008293TA29GENIChomozygous55263875
6118008916118008917GGC20GENIChomozygous55263878
6118008918118008926TGGTTGTG--------21GENIChomozygous55263880
6118008927118008928GC16GENIChomozygous55532889
6118008929118008930CCATT15GENIChomozygous55263883
6118009040118009042CC--8GENIChomozygous55263885
6118009751118009752GGA17GENIChomozygous55263888
6118009759118009760CA21GENIChomozygous55263890
6118010166118010167GT26GENIChomozygous55263892
6118010236118010237CT29GENIChomozygous55263895
6118011842118011843CT34GENIChomozygous55263897
6118012262118012263GT9GENIChomozygous55263900
6118012275118012276CG11GENIChomozygous55263902
6118012296118012297AG6GENIChomozygous55263905
6118012537118012538CT6GENIChomozygous55263907
6118007350118007351AAACACACAC11GENIChomozygous54960002