chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	97815625	97815626	G	A	24	GENIC	possibly homozygous	67126399
13	97816254	97816255	G	A	21	GENIC	homozygous	67126401
13	97816275	97816276	G	A	16	GENIC	homozygous	67126403
13	97816320	97816321	C	T	14	GENIC	homozygous	67126405
13	97817604	97817605	C		23	GENIC	heterozygous	66881818
13	97817655	97817656	T	C	18	GENIC	homozygous	66166266
13	97818491	97818492	T		16	GENIC	homozygous	67126409
13	97820945	97820946	A		3	GENIC	homozygous	67126411
13	97822347	97822348	G	A	13	GENIC	homozygous	67126413
13	97822473	97822474	A	G	9	GENIC	homozygous	67126415
13	97822505	97822506	A	G	8	GENIC	homozygous	67126417
13	97822820	97822821	A	T	7	GENIC	homozygous	67126419
13	97818079	97818080	A	T	4	GENIC	homozygous	67332775
13	97818491	97818492	T	A	4	GENIC	homozygous	67332777
13	97824082	97824083	T	A	20	GENIC	homozygous	67126421
13	97824648	97824649	C	T	18	GENIC	homozygous	67126423
13	97825001	97825002	T		13	GENIC	homozygous	67126425
13	97827349	97827350	T	C	19	GENIC	homozygous	67126429
13	97829015	97829015		T	29	GENIC	heterozygous	67332779
13	97830481	97830482	G	A	20	GENIC	homozygous	67126433
13	97830640	97830641	T	C	16	GENIC	homozygous	67126435
13	97831511	97831512	C	T	6	GENIC	homozygous	67126437
13	97831779	97831781	CA		19	GENIC	heterozygous	67126439
13	97832059	97832060	G		20	GENIC	possibly homozygous	67126441
13	97832743	97832744	A	G	4	GENIC	homozygous	67126443
13	97832948	97832949	T	C	15	GENIC	homozygous	67126445
13	97833078	97833079	T	C	21	GENIC	homozygous	67126447
13	97833232	97833233	T		15	GENIC	heterozygous	67126451
13	97834462	97834463	A		11	GENIC	heterozygous	67126453
13	97834580	97834581	A	T	22	GENIC	homozygous	67126455
13	97834656	97834657	T	C	19	GENIC	homozygous	67126457