chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	49737093	49737094	A	G	13	GENIC	homozygous	50234379
12	49739599	49739600	G	A	10	GENIC	homozygous	50234388
12	49747293	49747294	T	-	7	GENIC	homozygous	50234392
12	49753758	49753759	A	G	13	GENIC	homozygous	50234400
12	49753765	49753766	T	C	13	GENIC	homozygous	50234402
12	49755576	49755577	C	T	13	GENIC	homozygous	50234404
12	49756017	49756018	C	T	10	GENIC	homozygous	50234406
12	49756865	49756866	C	T	19	GENIC	homozygous	50234408
12	49757132	49757133	G	GTGAA	11	GENIC	homozygous	50234410
12	49757342	49757343	C	G	17	GENIC	homozygous	50234412
12	49760336	49760337	C	G	13	GENIC	homozygous	50234414
12	49762437	49762438	G	A	7	GENIC	homozygous	50234416
12	49762446	49762447	G	T	8	GENIC	homozygous	50234418
12	49763321	49763322	T	G	9	GENIC	homozygous	50234420
12	49769453	49769454	T	C	12	GENIC	homozygous	50234450
12	49770203	49770204	G	A	9	GENIC	homozygous	50234452
12	49770351	49770352	A	AT	11	GENIC	homozygous	50234454
12	49773062	49773063	T	C	9	GENIC	homozygous	50234458
12	49773210	49773211	C	T	14	GENIC	homozygous	50234460
12	49773598	49773599	C	A	10	GENIC	homozygous	50234462
12	49774225	49774226	A	G	8	GENIC	homozygous	50234464
12	49777221	49777222	T	C	8	GENIC	homozygous	50234470
12	49777242	49777243	T	C	11	GENIC	homozygous	50234472
12	49778862	49778863	A	G	7	GENIC	homozygous	50234476