chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	49299472	49299473	A	T	21	GENIC	homozygous	116882342
10	49305587	49305588	G	T	30	GENIC	homozygous	116882354
10	49306394	49306395	G	T	11	GENIC	homozygous	116882356
10	49306455	49306456	A	G	33	GENIC	homozygous	116882358
10	49309328	49309329	G	A	28	GENIC	homozygous	116882366
10	49309430	49309431	C	T	24	GENIC	homozygous	116882368
10	49309642	49309643	G	C	6	GENIC	homozygous	118037089
10	49309597	49309598	A	G	9	GENIC	homozygous	117009404
10	49309599	49309600	C	T	9	GENIC	homozygous	117009405
10	49310546	49310547	G	A	29	GENIC	homozygous	116882370
10	49310864	49310865	C	T	22	GENIC	homozygous	116882372
10	49310922	49310923	A	G	21	GENIC	homozygous	116882374
10	49311144	49311145	C	G	15	GENIC	homozygous	116882376
10	49311200	49311201	G	T	17	GENIC	homozygous	116882378
10	49311257	49311258	T	C	28	GENIC	homozygous	116882380
10	49311532	49311533	G	A	10	GENIC	homozygous	116882382
10	49311767	49311768	C	T	21	GENIC	homozygous	116882384
10	49312527	49312528	T	C	9	GENIC	homozygous	117078236
10	49312532	49312533	T	C	7	GENIC	homozygous	116882386
10	49311891	49311892	C	T	17	GENIC	homozygous	116588742
10	49311899	49311900	A	T	15	GENIC	homozygous	116588744