chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	31462060	31462061	T	C	22	GENIC	homozygous	116546588
10	31468013	31468014	A	G	18	GENIC	homozygous	126379922
10	31474667	31474668	A	T	12	GENIC	homozygous	116546600
10	31486026	31486027	T	C	12	GENIC	homozygous	116546602
10	31486090	31486091	G	A	22	GENIC	homozygous	116546604
10	31486805	31486806	T	G	20	GENIC	homozygous	116752477
10	31487119	31487120	C	T	15	GENIC	homozygous	116546606
10	31487600	31487601	G	A	14	GENIC	homozygous	116546608
10	31487731	31487732	C	T	25	GENIC	homozygous	116546610
10	31488533	31488534	A	G	9	GENIC	homozygous	116546612
10	31488690	31488691	G	A	19	GENIC	homozygous	116546614
10	31488718	31488719	G	T	19	GENIC	homozygous	116546616
10	31488963	31488964	C	G	24	GENIC	homozygous	116546618
10	31489661	31489662	C	T	16	GENIC	homozygous	116546624
10	31489047	31489048	G	A	22	GENIC	homozygous	116546620
10	31489167	31489168	A	G	7	GENIC	homozygous	116546622
10	31490129	31490130	A	G	15	GENIC	homozygous	116546626
10	31491221	31491222	T	G	18	GENIC	homozygous	116546628
10	31491235	31491236	C	T	20	GENIC	homozygous	116546630
10	31491663	31491664	G	A	13	GENIC	homozygous	116752479
10	31492144	31492145	G	A	17	GENIC	homozygous	116546632
10	31492547	31492548	T	C	15	GENIC	homozygous	116546634
10	31492905	31492906	C	T	17	GENIC	homozygous	116546636
10	31493055	31493056	A	G	20	GENIC	homozygous	116546638
10	31493133	31493134	G	A	12	GENIC	homozygous	116546640