chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	23781525	23781526	A	C	24	GENIC	homozygous	133313749
17	23781804	23781805	C	T	46	GENIC	homozygous	119333286
17	23782546	23782547	C	T	61	GENIC	homozygous	111340101
17	23781941	23781942	C	T	49	GENIC	homozygous	111340093
17	23782075	23782076	A	G	53	GENIC	homozygous	111340095
17	23782094	23782095	C	A	55	GENIC	possibly homozygous	111340097
17	23782449	23782450	A	C	51	GENIC	homozygous	111340099
17	23782577	23782578	T	C	61	GENIC	homozygous	111340103
17	23782618	23782619	G	A	67	GENIC	homozygous	111340105
17	23782745	23782746	A	G	84	GENIC	homozygous	111340107
17	23782776	23782777	A	T	85	GENIC	homozygous	111340109
17	23782915	23782916	T	C	54	GENIC	homozygous	111340111
17	23783701	23783702	C	A	54	GENIC	possibly homozygous	119333288
17	23784860	23784861	A	G	58	GENIC	possibly homozygous	133313750
17	23784813	23784814	T	C	56	GENIC	homozygous	111497863
17	23785921	23785924	TAA		38	GENIC	homozygous	129436625
17	23787347	23787347		TGTGTGTCCAGCACG	43	GENIC	homozygous	129436627
17	23788106	23788107	C	A	44	GENIC	possibly homozygous	111340113
17	23788873	23788874	T	A	63	GENIC	possibly homozygous	110997784
17	23789850	23789851	T	C	40	GENIC	homozygous	110997798
17	23790126	23790127	A	C	53	GENIC	homozygous	110997802
17	23790127	23790128	A	C	53	GENIC	homozygous	110997805
17	23790338	23790339	A	G	49	GENIC	homozygous	110997813
17	23789042	23789043	T	C	58	GENIC	homozygous	111180421
17	23790598	23790599	G	T	31	GENIC	homozygous	110997815
17	23791144	23791145	C	T	54	GENIC	homozygous	110997821
17	23791210	23791211	G	A	60	GENIC	homozygous	110997825
17	23791982	23791983	T	C	58	GENIC	homozygous	111340115