chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	18510756	18510757	T	C	32	GENIC	homozygous	110978285
17	18510874	18510875	A	T	25	GENIC	homozygous	110978286
17	18510875	18510876	T	C	27	GENIC	homozygous	110978288
17	18511081	18511082	T	G	35	GENIC	homozygous	110978290
17	18511572	18511573	A	C	18	GENIC	homozygous	110978292
17	18512081	18512082	A	G	20	GENIC	homozygous	111175576
17	18512135	18512136	T	G	22	GENIC	homozygous	110978294
17	18512252	18512253	T	C	19	GENIC	homozygous	110978296
17	18512295	18512296	G	A	23	GENIC	homozygous	110978298
17	18512426	18512427	G	C	17	GENIC	homozygous	110978300
17	18512582	18512583	T	C	27	GENIC	homozygous	110978302
17	18512678	18512679	A	G	26	GENIC	homozygous	110978304
17	18512844	18512845	C	T	24	GENIC	homozygous	110978306
17	18513133	18513134	G	T	23	GENIC	homozygous	110978308
17	18513259	18513260	C	T	20	GENIC	homozygous	110978310
17	18513431	18513432	C	T	18	GENIC	homozygous	110978312
17	18513647	18513648	C	T	19	GENIC	homozygous	110978314
17	18513649	18513650	G	A	19	GENIC	homozygous	110978316
17	18513654	18513655	A	G	20	GENIC	homozygous	110978318
17	18513710	18513711	A	C	28	GENIC	homozygous	110978320
17	18513757	18513758	G	T	27	GENIC	homozygous	110978322
17	18514020	18514021	A	T	17	GENIC	homozygous	110978324
17	18514066	18514067	C	T	15	GENIC	homozygous	110978326