chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10586510	10586511	A	G	12	GENIC	homozygous	110954435
17	10587410	10587411	T	G	21	GENIC	homozygous	110954437
17	10587799	10587800	G	T	21	GENIC	homozygous	111231022
17	10588953	10588954	A	G	14	GENIC	homozygous	110954439
17	10589088	10589089	G	A	15	GENIC	homozygous	110954441
17	10593112	10593113	A	G	22	GENIC	homozygous	110954443
17	10593324	10593325	C	T	22	GENIC	homozygous	110954445
17	10593367	10593368	G	A	24	GENIC	homozygous	110954447
17	10593401	10593402	C	T	20	GENIC	homozygous	110954449
17	10593626	10593627	C	T	19	GENIC	homozygous	110954451
17	10593779	10593780	C	A	22	GENIC	homozygous	110954453
17	10594285	10594286	G	C	20	GENIC	homozygous	110954455
17	10594706	10594707	A	T	21	GENIC	homozygous	110954457
17	10594884	10594885	T	A	19	GENIC	homozygous	110954459
17	10594930	10594931	C	T	20	GENIC	homozygous	110954461
17	10595164	10595165	A	G	18	GENIC	homozygous	110954463
17	10595254	10595255	A	T	16	GENIC	homozygous	110954465
17	10595412	10595413	A	G	20	GENIC	homozygous	110954467
17	10595460	10595461	C	A	9	GENIC	homozygous	110954469
17	10595490	10595491	T	G	5	GENIC	homozygous	110954471
17	10596344	10596345	C	G	15	GENIC	homozygous	110954473
17	10596496	10596497	T	C	18	GENIC	homozygous	110954475
17	10596902	10596903	C	T	22	GENIC	homozygous	110954477
17	10597898	10597899	G	T	4	GENIC	homozygous	111315082
17	10598056	10598057	C	T	18	GENIC	homozygous	110954481
17	10598316	10598317	C	A	21	GENIC	homozygous	110954483