chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	37547469	37547470	G	C	11	GENIC	heterozygous	119362464
17	37547559	37547560	T	C	19	GENIC	homozygous	119362465
17	37548510	37548511	C	G	33	GENIC	heterozygous	119362466
17	37548685	37548686	A	G	37	GENIC	heterozygous	119362467
17	37548906	37548907	T	C	45	GENIC	heterozygous	119362468
17	37551590	37551591	G	A	29	GENIC	heterozygous	119362469
17	37553696	37553697	T	A	28	GENIC	homozygous	111038550
17	37558251	37558252	T	A	23	GENIC	homozygous	111304765
17	37563032	37563033	G	A	39	GENIC	heterozygous	119362470
17	37566959	37566960	C	G	22	GENIC	homozygous	119282495
17	37567481	37567482	C	A	29	GENIC	heterozygous	119362471
17	37573576	37573577	T	C	37	GENIC	homozygous	111038594
17	37577639	37577640	T	G	12	GENIC	homozygous	111038600
17	37584764	37584765	T	A	21	GENIC	homozygous	111304766
17	37589187	37589188	C	A	86	GENIC	heterozygous	119362472
17	37590009	37590010	G	A	24	GENIC	homozygous	111304767
17	37592809	37592810	G	A	13	GENIC	homozygous	119282513
17	37592896	37592897	C	T	11	GENIC	homozygous	119282515
17	37568785	37568786	G	C	21	GENIC	homozygous	111499791
17	37568789	37568790	G	C	20	GENIC	homozygous	111499793
17	37586833	37586834	A	C	13	GENIC	possibly homozygous	111317994
17	37593280	37593281	T	C	19	GENIC	homozygous	111199229
17	37593451	37593452	T	A	19	GENIC	homozygous	119282519
17	37596569	37596570	T	C	18	GENIC	homozygous	111038622
17	37596936	37596937	A	T	27	GENIC	homozygous	111304768
17	37601239	37601240	A	G	15	GENIC	homozygous	111038626
17	37601469	37601470	T	C	22	GENIC	homozygous	111038628
17	37602822	37602823	A	T	17	GENIC	homozygous	111038630
17	37604269	37604270	A	G	19	GENIC	homozygous	111038634
17	37605415	37605416	G	A	33	GENIC	homozygous	111304769
17	37606030	37606031	T	C	22	GENIC	homozygous	111304770
17	37606337	37606338	C	A	27	GENIC	homozygous	111038636
17	37606883	37606884	T	C	29	GENIC	homozygous	111038644
17	37608126	37608127	A	T	26	GENIC	homozygous	111038646
17	37610227	37610228	G	T	18	GENIC	homozygous	111304771