chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	50269890	50269891	C	G	13	GENIC	homozygous	115444423
12	50270580	50270581	G	A	24	GENIC	homozygous	115549285
12	50271551	50271552	G	A	36	GENIC	homozygous	115549287
12	50273093	50273094	C	T	37	GENIC	possibly homozygous	115549289
12	50274744	50274745	G	A	30	GENIC	homozygous	115549291
12	50275500	50275501	A	G	30	GENIC	homozygous	115403385
12	50273740	50273741	T	G	20	GENIC	homozygous	115351946
12	50276078	50276079	A	G	20	GENIC	homozygous	115403387
12	50278796	50278797	A	G	38	GENIC	homozygous	115403389
12	50279362	50279363	T	A	37	GENIC	homozygous	115403391