chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	7058562	7058563	A	G	43	GENIC	homozygous	116731853
10	7059230	7059231	T	C	34	GENIC	homozygous	116731854
10	7060849	7060850	T	C	40	GENIC	homozygous	116731855
10	7060905	7060906	T	C	32	GENIC	homozygous	116731856
10	7060943	7060944	A	G	30	GENIC	homozygous	116731857
10	7061143	7061144	G	A	51	GENIC	homozygous	116731858
10	7063060	7063061	A	G	50	GENIC	homozygous	116731859
10	7064321	7064322	A	G	48	GENIC	homozygous	116731860
10	7064836	7064837	G	A	39	GENIC	homozygous	116731861
10	7064911	7064912	G	A	35	GENIC	homozygous	116731862
10	7065058	7065059	C	T	48	GENIC	homozygous	116482245
10	7065624	7065625	A	G	37	GENIC	possibly homozygous	116482247
10	7068388	7068389	T	C	32	GENIC	homozygous	116731863
10	7068490	7068491	C	T	47	GENIC	homozygous	116731864
10	7070106	7070107	C	A	54	GENIC	homozygous	116731865
10	7071068	7071069	T	G	63	GENIC	homozygous	116482249
10	7071340	7071341	G	A	49	GENIC	possibly homozygous	116731866
10	7071692	7071693	A	T	42	GENIC	homozygous	116731867
10	7072212	7072213	T	C	38	GENIC	homozygous	116731868
10	7076323	7076324	A	G	56	GENIC	homozygous	116731869
10	7074169	7074170	C	T	45	GENIC	homozygous	117119098
10	7067388	7067389	G	A	37	GENIC	homozygous	117119096