chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	2845659	2845660	A	G	37	GENIC	homozygous	130017423
20	2845896	2845897	A	G	28	GENIC	homozygous	130017424
20	2847295	2847296	C	T	26	GENIC	homozygous	140504080
20	2847363	2847364	T	C	40	GENIC	homozygous	140504081
20	2848699	2848700	C	A	40	GENIC	homozygous	140504082
20	2849624	2849625	G	A	30	GENIC	homozygous	140504083
20	2850925	2850926	A	G	46	GENIC	possibly homozygous	130017425
20	2852767	2852768	G	T	26	GENIC	homozygous	130017426
20	2855123	2855124	G	A	44	GENIC	homozygous	130017427
20	2856282	2856283	T	C	47	GENIC	homozygous	130017428
20	2856545	2856546	C	T	45	GENIC	homozygous	130017429
20	2857058	2857059	T	G	42	GENIC	homozygous	130017430
20	2857484	2857484		TCAT	22	GENIC	homozygous	140482006