chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	43774948	43774949	A	G	40	GENIC	homozygous	111053624
17	43775667	43775668	G	C	39	GENIC	homozygous	111053626
17	43775845	43775846	G	A	26	GENIC	homozygous	111053628
17	43776736	43776737	T	C	29	GENIC	homozygous	111053630
17	43776863	43776864	A	G	29	GENIC	homozygous	111053632
17	43777333	43777334	T	G	21	GENIC	homozygous	111318424
17	43779103	43779104	C	A	40	GENIC	homozygous	111053636
17	43781465	43781466	G	A	29	GENIC	homozygous	111053639
17	43781709	43781710	C	T	40	GENIC	homozygous	111053641
17	43784250	43784251	T	C	40	GENIC	homozygous	111053643
17	43784947	43784948	G	C	51	GENIC	homozygous	111053645
17	43789433	43789434	C	A	15	GENIC	homozygous	111053647
17	43792969	43792970	C	G	29	GENIC	homozygous	111053649
17	43793563	43793564	T	A	23	GENIC	homozygous	111053651
17	43794745	43794746	T	G	33	GENIC	homozygous	111053653
17	43794751	43794752	T	G	36	GENIC	homozygous	111053657
17	43796516	43796517	G	A	32	GENIC	homozygous	111053659
17	43796639	43796640	G	C	26	GENIC	homozygous	111053661
17	43797006	43797007	C	T	39	GENIC	homozygous	111053663
17	43798793	43798794	G	A	46	GENIC	homozygous	111053667
17	43799655	43799656	T	C	37	GENIC	homozygous	111053669
17	43800273	43800274	G	A	31	GENIC	homozygous	111053671
17	43801516	43801517	C	T	39	GENIC	possibly homozygous	111053675
17	43803107	43803108	T	C	29	GENIC	homozygous	111053677
17	43805122	43805123	T	C	25	GENIC	homozygous	111053681
17	43806907	43806908	G	A	51	GENIC	homozygous	111053683
17	43808620	43808621	A	C	37	GENIC	homozygous	111053687
17	43814651	43814652	T	G	35	GENIC	homozygous	111053689
17	43816380	43816381	T	C	36	GENIC	homozygous	111053691
17	43816441	43816442	A	G	33	GENIC	homozygous	111053693
17	43784004	43784005	C	A	29	GENIC	homozygous	111244713
17	43791354	43791355	A	C	34	GENIC	homozygous	111244717
17	43817143	43817144	A	C	29	GENIC	homozygous	111204018