chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	48376061	48376062	C	T	34	GENIC	homozygous	51639340
10	48377628	48377629	T	TGAA	33	GENIC	homozygous	51639342
10	48378655	48378656	A	G	20	GENIC	homozygous	51639343
10	48379162	48379163	A	-	29	GENIC	homozygous	51639344
10	48379781	48379782	T	C	23	GENIC	homozygous	52055456
10	48379904	48379905	A	-	17	GENIC	possibly homozygous	51639345
10	48380698	48380699	T	C	31	GENIC	homozygous	51639346
10	48381003	48381004	T	C	33	GENIC	homozygous	51639347
10	48381288	48381289	C	T	25	GENIC	homozygous	51639348
10	48381371	48381372	T	C	24	GENIC	homozygous	51639349
10	48382096	48382097	C	T	33	GENIC	homozygous	51639350
10	48382213	48382214	T	G	30	GENIC	homozygous	51639351
10	48382594	48382595	A	-	14	GENIC	homozygous	51639352
10	48382615	48382616	T	TGG	22	GENIC	homozygous	51639353
10	48382644	48382645	C	T	26	GENIC	possibly homozygous	51639354
10	48384221	48384222	A	ACC	11	GENIC	homozygous	51639355
10	48386597	48386598	G	A	17	GENIC	homozygous	51639359
10	48387170	48387171	C	A	25	GENIC	homozygous	51639360
10	48387179	48387180	C	T	23	GENIC	homozygous	51639361