chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3042706	3042707	T	C	72	GENIC	homozygous	142719921
20	3051566	3051567	C	T	46	GENIC	homozygous	142719922
20	3051931	3051932	T	A	56	GENIC	homozygous	130017781
20	3046803	3046804	T	C	64	GENIC	homozygous	130017776
20	3047313	3047314	C	T	58	GENIC	homozygous	130017777
20	3050115	3050116	A	G	58	GENIC	homozygous	130017779
20	3050640	3050641	T	G	49	GENIC	homozygous	130017780
20	3048867	3048871	TTTC		43	GENIC	possibly homozygous	142711270
20	3055514	3055515	C		11	GENIC	homozygous	403456316
20	3055514	3055515	C	T	11	GENIC	heterozygous	403456317
20	3055512	3055513	C		11	GENIC	homozygous	403456314
20	3055512	3055513	C	T	11	GENIC	heterozygous	403456315
20	3055516	3055517	C		11	GENIC	homozygous	403456318
20	3055516	3055517	C	T	11	GENIC	heterozygous	403456319
20	3055518	3055519	C		11	GENIC	homozygous	403456320
20	3055518	3055519	C	T	11	GENIC	heterozygous	403456321
20	3058002	3058002		TG	41	GENIC	homozygous	129976673
20	3059622	3059623	G	A	54	GENIC	homozygous	142719923
20	3062344	3062345	G	A	57	GENIC	homozygous	130017784