chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	29997762	29997763	C	A	10	GENIC	possibly homozygous	45510508
20	29999247	29999248	A	G	5	GENIC	heterozygous	45510509
20	29999569	29999570	G	A	4	GENIC	homozygous	45510520
20	30000940	30000942	GA	--	15	GENIC	possibly homozygous	45510522
20	30001152	30001153	T	C	24	GENIC	homozygous	45510524
20	30003584	30003585	C	A	26	GENIC	possibly homozygous	45510528
20	30004117	30004118	G	T	13	GENIC	homozygous	45510530
20	30004120	30004121	G	A	16	GENIC	homozygous	45510532
20	30004649	30004650	G	A	21	GENIC	possibly homozygous	45510534
20	30005237	30005238	A	AG	13	GENIC	possibly homozygous	45701842
20	30005267	30005268	A	T	15	GENIC	possibly homozygous	45701843
20	30007141	30007142	G	T	36	GENIC	homozygous	45701846
20	30009338	30009339	A	G	17	GENIC	homozygous	45510557
20	30009957	30009958	A	G	21	GENIC	homozygous	45510565
20	30010596	30010597	C	T	23	GENIC	possibly homozygous	45701847
20	30012863	30012864	G	A	8	GENIC	homozygous	45701848
20	30012864	30012865	C	A	8	GENIC	homozygous	45701849
20	30012910	30012911	T	C	19	GENIC	homozygous	45510569
20	30024650	30024651	T	C	27	GENIC	possibly homozygous	45510593
20	30025195	30025196	C	T	12	GENIC	homozygous	45701850
20	30029402	30029403	G	A	38	GENIC	possibly homozygous	45701851
20	30032126	30032127	A	G	18	GENIC	homozygous	45510638
20	30032248	30032249	C	T	21	GENIC	homozygous	45701852
20	30033456	30033457	A	G	18	GENIC	homozygous	45510644
20	30036965	30036966	G	T	28	GENIC	homozygous	45701853
20	30038127	30038128	G	-	22	GENIC	homozygous	45701854
20	30048441	30048442	C	-	14	GENIC	homozygous	45701858
20	30050013	30050014	A	G	19	GENIC	homozygous	45822070
20	30053552	30053553	C	T	22	GENIC	homozygous	45701859
20	30064263	30064264	T	C	11	GENIC	homozygous	45510811
20	30066886	30066887	T	C	23	GENIC	possibly homozygous	45701864
20	30078024	30078025	A	AC	3	GENIC	homozygous	45701867
20	30078147	30078148	A	G	11	GENIC	possibly homozygous	45701868
20	30078862	30078863	A	AG	20	GENIC	homozygous	45510903