chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	15586489	15586490	T	C	23	GENIC	homozygous	111171663
17	15586611	15586612	G	A	27	GENIC	homozygous	111171665
17	15588530	15588531	A	G	26	GENIC	homozygous	111171667
17	15588803	15588804	G	A	20	GENIC	homozygous	111171669
17	15588840	15588841	T	C	21	GENIC	homozygous	111171671
17	15588856	15588857	A	G	23	GENIC	homozygous	111171673
17	15588891	15588892	A	G	29	GENIC	homozygous	111171677
17	15588901	15588902	G	C	32	GENIC	homozygous	111171679
17	15588970	15588971	T	C	26	GENIC	homozygous	111171681
17	15589033	15589034	A	G	23	GENIC	homozygous	111171683
17	15589102	15589103	A	G	21	GENIC	homozygous	111171685
17	15589472	15589473	A	C	15	GENIC	homozygous	111171687
17	15589664	15589665	T	C	16	GENIC	homozygous	111171689
17	15591082	15591083	A	C	23	GENIC	homozygous	111171691
17	15591202	15591203	T	C	18	GENIC	homozygous	111171693
17	15591311	15591312	T	G	12	GENIC	homozygous	111171695
17	15593038	15593039	A	G	13	GENIC	homozygous	111171697