chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10586126	10586127	C	A	32	GENIC	homozygous	110954433
17	10586510	10586511	A	G	49	GENIC	homozygous	110954435
17	10587410	10587411	T	G	23	GENIC	homozygous	110954437
17	10587799	10587800	G	T	25	GENIC	homozygous	111231022
17	10588953	10588954	A	G	39	GENIC	homozygous	110954439
17	10589088	10589089	G	A	37	GENIC	homozygous	110954441
17	10593112	10593113	A	G	26	GENIC	homozygous	110954443
17	10593324	10593325	C	T	36	GENIC	homozygous	110954445
17	10593367	10593368	G	A	38	GENIC	homozygous	110954447
17	10593401	10593402	C	T	48	GENIC	homozygous	110954449
17	10593626	10593627	C	T	34	GENIC	homozygous	110954451
17	10593779	10593780	C	A	27	GENIC	homozygous	110954453
17	10594285	10594286	G	C	38	GENIC	homozygous	110954455
17	10594706	10594707	A	T	19	GENIC	homozygous	110954457
17	10594884	10594885	T	A	14	GENIC	homozygous	110954459
17	10594930	10594931	C	T	13	GENIC	homozygous	110954461
17	10595164	10595165	A	G	24	GENIC	homozygous	110954463
17	10595254	10595255	A	T	26	GENIC	homozygous	110954465
17	10595412	10595413	A	G	32	GENIC	homozygous	110954467
17	10595460	10595461	C	A	32	GENIC	homozygous	110954469
17	10596344	10596345	C	G	44	GENIC	homozygous	110954473
17	10596496	10596497	T	C	33	GENIC	homozygous	110954475
17	10596902	10596903	C	T	36	GENIC	homozygous	110954477
17	10597816	10597817	T	G	24	GENIC	homozygous	110954479
17	10597824	10597825	C	T	22	GENIC	homozygous	111231024
17	10598056	10598057	C	T	33	GENIC	homozygous	110954481
17	10598316	10598317	C	A	36	GENIC	homozygous	110954483