chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37991483	37991484	A	T	26	GENIC	homozygous	109694720
19	37991512	37991513	G	C	20	GENIC	homozygous	109694722
19	37991765	37991766	A	C	31	GENIC	homozygous	109694724
19	37992240	37992241	T	G	13	GENIC	homozygous	119629294
19	37993178	37993179	G	A	31	GENIC	homozygous	109694726
19	37993527	37993528	C	T	45	GENIC	homozygous	109925098
19	37993851	37993852	A	G	19	GENIC	homozygous	109694728
19	37993982	37993983	C	T	15	GENIC	heterozygous	119629295
19	37994004	37994005	G	T	12	GENIC	homozygous	119629296
19	37994894	37994895	G	A	43	GENIC	homozygous	109694730
19	37995366	37995367	A	T	46	GENIC	homozygous	109694732
19	37995373	37995374	A	G	44	GENIC	homozygous	109694734
19	37995773	37995774	C	T	30	GENIC	homozygous	109694736
19	37995784	37995785	C	T	33	GENIC	homozygous	109694738
19	37995937	37995938	G	A	31	GENIC	homozygous	109694740
19	37996012	37996013	G	A	56	GENIC	homozygous	109694742
19	37996466	37996467	T	C	30	GENIC	homozygous	119629297
19	37996811	37996812	T	A	16	GENIC	homozygous	109925102
19	37998323	37998324	T	C	28	GENIC	homozygous	119629298
19	37998327	37998328	C	A	28	GENIC	homozygous	119629299
19	37995152	37995153	T	G	44	GENIC	possibly homozygous	110049511
19	37998704	37998705	G	C	46	GENIC	homozygous	109694744
19	37998721	37998722	T	C	45	GENIC	homozygous	109694746
19	37998784	37998785	G	A	37	GENIC	homozygous	109694748
19	37998672	37998673	A	T	47	GENIC	homozygous	110065544
19	38030282	38030283	T	G	27	GENIC	heterozygous	109694750