chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	66341936	66341937	C	A	15	GENIC	homozygous	51479540
10	66342188	66342189	A	AGAGGCCTGGGTTCTTTTTTTTTTTTTTGAGCTGGGGACCGAACCCAGGGCTTTGTGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC	6	GENIC	heterozygous	52382616
10	66342188	66342189	A	AGAGGCCTGGGTTCTTTTTTTTTTTTTTTGAGCTGGGGACCGAACCCAGGGCTTTGTGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC	6	GENIC	heterozygous	52724633
10	66343029	66343030	C	T	20	GENIC	homozygous	51479541
10	66350666	66350667	A	G	20	GENIC	homozygous	51479543
10	66350764	66350765	A	ATTTTTT	13	GENIC	homozygous	51907945
10	66351483	66351484	C	T	16	GENIC	homozygous	51479547
10	66351527	66351528	G	A	16	GENIC	homozygous	51907947
10	66352061	66352062	T	A	21	GENIC	homozygous	51479548
10	66352225	66352226	G	A	26	GENIC	homozygous	51479549
10	66352692	66352693	T	-	4	GENIC	heterozygous	51907949
10	66353719	66353720	C	T	7	GENIC	homozygous	51479554
10	66354076	66354077	G	-	11	GENIC	homozygous	51907951
10	66354336	66354337	G	A	27	GENIC	homozygous	51479561
10	66354736	66354737	A	G	17	GENIC	homozygous	51479562
10	66354841	66354856	TGCCCTCTTCTGGTG	---------------	11	GENIC	homozygous	51479563
10	66354898	66354899	T	TAA	13	GENIC	homozygous	52382620
10	66354911	66354915	AACC	----	13	GENIC	homozygous	52382622
10	66354929	66354930	C	A	13	GENIC	homozygous	52382624
10	66354930	66354931	C	A	14	GENIC	homozygous	51907953
10	66355017	66355018	A	-	11	GENIC	homozygous	51479566
10	66355169	66355170	C	CAAAA	5	GENIC	heterozygous	51479567
10	66355169	66355170	C	CAA	5	GENIC	heterozygous	52503853
10	66355372	66355373	T	TA	16	GENIC	homozygous	51479568
10	66355389	66355390	A	-	19	GENIC	homozygous	51907955
10	66355414	66355415	G	T	26	GENIC	homozygous	51479569
10	66355454	66355455	C	A	24	GENIC	homozygous	51678708