chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	41882835	41882836	G	A	20	GENIC	homozygous	114541444
13	41883899	41883900	G	C	11	GENIC	homozygous	114329960
13	41883953	41883954	G	A	20	GENIC	homozygous	114541448
13	41883989	41883990	A	G	17	GENIC	homozygous	114541450
13	41885147	41885148	C	T	27	GENIC	homozygous	114541452
13	41886071	41886072	A	T	21	GENIC	homozygous	114541454
13	41886481	41886482	T	A	35	GENIC	homozygous	114541456
13	41887128	41887129	A	G	24	GENIC	homozygous	114541458
13	41887949	41887950	T	C	19	GENIC	homozygous	115136914
13	41888528	41888529	C	T	16	GENIC	homozygous	114541460
13	41888825	41888826	G	A	11	GENIC	homozygous	114541462
13	41901233	41901234	C	T	25	GENIC	homozygous	114541470
13	41903021	41903022	C	T	25	GENIC	homozygous	114921700
13	41906943	41906944	T	C	27	GENIC	homozygous	114541472
13	41907445	41907446	T	C	25	GENIC	homozygous	114541474
13	41910508	41910509	C	T	27	GENIC	homozygous	114541480
13	41920229	41920230	A	G	32	GENIC	homozygous	114541498
13	41884301	41884302	T	C	38	GENIC	homozygous	114754563