chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	95386608	95386609	T	C	30	GENIC	homozygous	68186957
10	95386711	95386712	A	G	34	GENIC	homozygous	68186961
10	95386752	95386753	A	T	27	GENIC	homozygous	68186964
10	95387091	95387092	C	T	22	GENIC	homozygous	68471394
10	95387143	95387144	A	G	23	GENIC	homozygous	68186967
10	95387349	95387350	G	A	55	GENIC	homozygous	68471397
10	95387836	95387837	C	G	38	GENIC	homozygous	68186971
10	95388095	95388096	G	A	36	GENIC	homozygous	68186974
10	95388524	95388525	A	G	19	GENIC	homozygous	68186978
10	95389225	95389226	G	A	30	GENIC	homozygous	68186986
10	95391345	95391346	C	T	32	GENIC	possibly homozygous	68187053
10	95391392	95391393	G	A	14	GENIC	possibly homozygous	68471400
10	95391438	95391439	G	A	22	GENIC	heterozygous	68187057
10	95391741	95391742	C	T	39	GENIC	homozygous	68471403
10	95391846	95391847	C	T	31	GENIC	homozygous	68187065
10	95392045	95392046	C	G	21	GENIC	possibly homozygous	68471406
10	95392635	95392636	T	C	30	GENIC	homozygous	68471410
10	95394170	95394171	G	A	59	GENIC	homozygous	68471414
10	95394506	95394507	G	A	41	GENIC	homozygous	68471417
10	95394933	95394934	T	C	8	GENIC	homozygous	68187096
10	95395190	95395191	T	C	18	GENIC	homozygous	68471420
10	95395351	95395352	C	T	27	GENIC	homozygous	68471423
10	95396838	95396839	C	G	17	GENIC	homozygous	68187112
10	95396839	95396840	G	T	16	GENIC	possibly homozygous	68471426
10	95397373	95397374	C	T	75	GENIC	homozygous	68471428
10	95398082	95398083	A	G	29	GENIC	homozygous	68471432
10	95398099	95398100	C	T	31	GENIC	homozygous	68471435
10	95398264	95398265	A	G	32	GENIC	homozygous	68471438
10	95398569	95398570	T	C	33	GENIC	homozygous	68187119
10	95398645	95398646	C	T	62	GENIC	homozygous	68471440
10	95399339	95399340	G	A	31	GENIC	homozygous	68471443