chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	27653049	27653050	C	T	27	GENIC	homozygous	109247919
20	27656105	27656106	T	C	29	GENIC	homozygous	109247921
20	27657536	27657537	G	T	19	GENIC	homozygous	109310276
20	27658421	27658422	C	T	29	GENIC	homozygous	109247923
20	27658425	27658426	C	T	27	GENIC	homozygous	109247925
20	27659269	27659270	C	G	22	GENIC	homozygous	109247927
20	27659537	27659538	G	C	7	GENIC	homozygous	109310278
20	27660090	27660091	T	C	46	GENIC	homozygous	109247929
20	27661706	27661707	C	T	40	GENIC	homozygous	109247931
20	27662124	27662125	T	C	36	GENIC	homozygous	109247933
20	27664292	27664293	G	A	17	GENIC	homozygous	109247935
20	27664333	27664334	A	G	20	GENIC	homozygous	109247937
20	27664487	27664488	C	T	27	GENIC	homozygous	109247939
20	27665399	27665400	C	T	15	GENIC	homozygous	109247941
20	27665930	27665931	C	T	33	GENIC	homozygous	109247943
20	27666376	27666377	C	T	34	GENIC	homozygous	109247945
20	27667129	27667130	A	G	24	GENIC	homozygous	109247947
20	27669043	27669044	G	A	25	GENIC	homozygous	109247949
20	27669962	27669963	C	T	23	GENIC	homozygous	109247951
20	27670910	27670911	T	C	40	GENIC	homozygous	109247953
20	27672527	27672528	C	A	41	GENIC	homozygous	109247955