chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	2914063	2914064	A	T	12	GENIC	homozygous	130017517
20	2914121	2914122	A	C	16	GENIC	possibly homozygous	130017519
20	2914560	2914561	T	C	31	GENIC	homozygous	130017520
20	2914943	2914944	A	G	18	GENIC	homozygous	140504153
20	2914979	2914980	T	A	19	GENIC	homozygous	140504154
20	2915003	2915004	C	A	21	GENIC	homozygous	140504155
20	2915140	2915141	T	C	34	GENIC	homozygous	130017521
20	2915230	2915231	T	C	20	GENIC	homozygous	130017522
20	2915527	2915528	T	C	18	GENIC	homozygous	130017523
20	2916211	2916212	C	A	19	GENIC	homozygous	140504156
20	2916360	2916361	G	A	29	GENIC	homozygous	140504157
20	2916436	2916437	G	A	28	GENIC	homozygous	140504158