chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	95761933	95761934	A	G	20	GENIC	homozygous	114908931
6	95763381	95763382	A	T	19	GENIC	homozygous	114908932
6	95763911	95763912	A	T	21	GENIC	homozygous	114908933
6	95764833	95764834	G	C	10	GENIC	homozygous	114908934
6	95765847	95765848	C	A	11	GENIC	homozygous	114908936
6	95768498	95768499	A	G	15	GENIC	homozygous	114908937
6	95769279	95769280	A		12	GENIC	possibly homozygous	128370060
6	95769456	95769457	T	C	13	GENIC	homozygous	114908938
6	95769672	95769673	C	T	13	GENIC	homozygous	114908939
6	95770985	95770986	G	A	9	GENIC	homozygous	114908940
6	95772424	95772425	A		24	GENIC	homozygous	128370061
6	95773948	95773949	G	A	14	GENIC	homozygous	114908941
6	95774021	95774022	A	G	12	GENIC	homozygous	114908942
6	95775616	95775617	C	T	12	GENIC	homozygous	114908943
6	95776554	95776555	C	T	16	GENIC	homozygous	114908944
6	95777015	95777016	C	T	20	GENIC	homozygous	114908945
6	95777790	95777791	A	G	14	GENIC	homozygous	114908946
6	95780267	95780267		TCCT	13	GENIC	homozygous	128370062
6	95781046	95781047	A	G	20	GENIC	homozygous	114908949
6	95781309	95781309		C	14	GENIC	homozygous	128370063
6	95786874	95786874		G	9	GENIC	homozygous	128370064
6	95791214	95791214		A	9	GENIC	homozygous	128370065
6	95792765	95792766	A	C	17	GENIC	homozygous	114908955
6	95782507	95782508	A	G	24	GENIC	homozygous	114908950
6	95784161	95784162	A	G	15	GENIC	homozygous	114908951
6	95786884	95786885	C	G	12	GENIC	homozygous	115072906
6	95788899	95788900	G	A	16	GENIC	homozygous	114908953
6	95794252	95794253	A	G	18	GENIC	homozygous	114908956
6	95794895	95794895		A	14	GENIC	possibly homozygous	128370066
6	95795273	95795274	G	A	17	GENIC	homozygous	114908957