chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	59800779	59800780	C		33	GENIC	homozygous	131574366
1	59801943	59801944	C	T	41	GENIC	homozygous	109412709
1	59802953	59802954	C	T	33	GENIC	homozygous	108116646
1	59803277	59803278	C	T	43	GENIC	homozygous	108116659
1	59803460	59803461	C	G	35	GENIC	homozygous	109412710
1	59803512	59803513	G	A	34	GENIC	homozygous	109412711
1	59803846	59803847	G	A	43	GENIC	homozygous	109412712
1	59804539	59804539		AC	27	GENIC	homozygous	127388515
1	59805528	59805529	G	C	42	GENIC	homozygous	108116695
1	59805575	59805576	C	T	41	GENIC	homozygous	108116696
1	59805585	59805586	T	G	39	GENIC	homozygous	109412713
1	59805587	59805588	G	A	40	GENIC	homozygous	109412714
1	59805798	59805799	C	A	30	GENIC	homozygous	109412715
1	59806214	59806328	GATATGTATCTTTTTTTTTTTTGGGGGGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC		10	GENIC	heterozygous	127388516
1	59809223	59809243	ATAGATAGATAGATAGATAC		37	GENIC	homozygous	133367576
1	59806940	59806941	G	A	34	GENIC	homozygous	120847376