chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	28990738	28990739	C	G	13	GENIC	homozygous	109157985
20	28991108	28991109	C	T	14	GENIC	homozygous	109249797
20	28992068	28992069	C	T	15	GENIC	homozygous	109249799
20	28992154	28992155	G	A	19	GENIC	homozygous	109249801
20	28992254	28992255	G	A	21	GENIC	homozygous	109249803
20	28992352	28992353	A	G	11	GENIC	homozygous	109249805
20	28993372	28993373	C	G	21	GENIC	homozygous	109249809
20	28993939	28993940	G	A	16	GENIC	homozygous	109249811
20	28994603	28994604	G	A	14	GENIC	homozygous	109310441
20	28995966	28995967	T	G	4	GENIC	homozygous	109158007
20	28996030	28996031	A	C	5	GENIC	homozygous	109249813
20	28996532	28996533	G	A	10	GENIC	homozygous	109158011
20	28996543	28996544	C	A	11	GENIC	homozygous	109249815
20	28996877	28996878	C	T	10	GENIC	homozygous	109249817
20	28997137	28997138	A	G	13	GENIC	homozygous	109158017
20	28997770	28997771	T	C	21	GENIC	homozygous	109158019
20	28998903	28998904	A	G	25	GENIC	homozygous	109249819
20	29000784	29000785	C	G	17	GENIC	homozygous	109158031
20	29004478	29004479	C	T	19	GENIC	homozygous	109249821
20	29005287	29005288	G	A	22	GENIC	homozygous	109158059
20	29005384	29005385	A	C	13	GENIC	homozygous	109158061
20	29005606	29005607	C	T	17	GENIC	homozygous	109249823
20	29006315	29006316	T	C	17	GENIC	homozygous	109249825
20	29007870	29007871	G	A	19	GENIC	homozygous	109249827