chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	31453699	31453700	G	T	17	GENIC	possibly homozygous	116546580
10	31453711	31453712	A	G	18	GENIC	homozygous	116546582
10	31453722	31453723	A	G	17	GENIC	homozygous	116546584
10	31453737	31453738	A	G	19	GENIC	homozygous	116546586
10	31462060	31462061	T	C	21	GENIC	homozygous	116546588
10	31465014	31465015	G	T	19	GENIC	possibly homozygous	116546590
10	31465048	31465049	C	G	12	GENIC	homozygous	116546592
10	31465050	31465051	G	T	12	GENIC	homozygous	116546594
10	31465400	31465401	A	C	22	GENIC	homozygous	116546596
10	31474667	31474668	A	T	25	GENIC	homozygous	116546600
10	31486026	31486027	T	C	26	GENIC	homozygous	116546602
10	31486090	31486091	G	A	30	GENIC	homozygous	116546604
10	31487119	31487120	C	T	29	GENIC	homozygous	116546606
10	31487600	31487601	G	A	23	GENIC	homozygous	116546608
10	31487731	31487732	C	T	37	GENIC	homozygous	116546610
10	31488533	31488534	A	G	18	GENIC	homozygous	116546612
10	31488690	31488691	G	A	24	GENIC	homozygous	116546614
10	31488718	31488719	G	T	25	GENIC	homozygous	116546616
10	31488963	31488964	C	G	22	GENIC	homozygous	116546618
10	31489047	31489048	G	A	26	GENIC	homozygous	116546620
10	31489167	31489168	A	G	23	GENIC	homozygous	116546622
10	31489661	31489662	C	T	27	GENIC	homozygous	116546624
10	31490129	31490130	A	G	32	GENIC	homozygous	116546626
10	31491221	31491222	T	G	30	GENIC	homozygous	116546628
10	31491235	31491236	C	T	29	GENIC	homozygous	116546630
10	31492144	31492145	G	A	39	GENIC	homozygous	116546632
10	31492547	31492548	T	C	24	GENIC	homozygous	116546634
10	31492905	31492906	C	T	17	GENIC	homozygous	116546636
10	31493055	31493056	A	G	22	GENIC	homozygous	116546638
10	31493133	31493134	G	A	28	GENIC	homozygous	116546640
10	31486805	31486806	T	G	31	GENIC	homozygous	116752477
10	31491663	31491664	G	A	27	GENIC	homozygous	116752479