chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	39096234	39096235	T	C	31	GENIC	homozygous	111042108
17	39096239	39096240	A	G	30	GENIC	homozygous	111042110
17	39096620	39096621	C	T	26	GENIC	homozygous	111201162
17	39098126	39098127	T	G	21	GENIC	homozygous	111042112
17	39099072	39099073	T	A	26	GENIC	homozygous	111042114
17	39100720	39100721	C	T	34	GENIC	homozygous	111042116
17	39101126	39101127	T	C	28	GENIC	homozygous	111042118
17	39101426	39101427	A	G	24	GENIC	homozygous	111042120
17	39101717	39101718	C	T	32	GENIC	homozygous	111042122
17	39102427	39102428	A	T	19	GENIC	homozygous	111042124
17	39102680	39102681	T	C	30	GENIC	homozygous	111042126
17	39102861	39102862	A	G	21	GENIC	homozygous	111201165
17	39102891	39102892	G	T	26	GENIC	homozygous	111042128
17	39103202	39103203	G	A	22	GENIC	homozygous	111042130
17	39103272	39103273	G	C	16	GENIC	homozygous	111201166
17	39103307	39103308	G	A	13	GENIC	homozygous	111042132
17	39103591	39103592	A	T	23	GENIC	homozygous	111042134
17	39103784	39103785	G	A	28	GENIC	homozygous	111201167
17	39103805	39103806	C	T	31	GENIC	homozygous	111201168