chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	41882835	41882836	G	A	3	GENIC	homozygous	114541444
13	41883899	41883900	G	C	19	GENIC	homozygous	114329960
13	41883953	41883954	G	A	23	GENIC	homozygous	114541448
13	41883989	41883990	A	G	17	GENIC	homozygous	114541450
13	41885147	41885148	C	T	24	GENIC	homozygous	114541452
13	41886071	41886072	A	T	20	GENIC	homozygous	114541454
13	41886481	41886482	T	A	12	GENIC	homozygous	114541456
13	41887128	41887129	A	G	21	GENIC	homozygous	114541458
13	41888528	41888529	C	T	22	GENIC	homozygous	114541460
13	41888825	41888826	G	A	29	GENIC	homozygous	114541462
13	41901233	41901234	C	T	23	GENIC	homozygous	114541470
13	41903021	41903022	C	T	28	GENIC	homozygous	114921700
13	41906943	41906944	T	C	17	GENIC	homozygous	114541472
13	41907445	41907446	T	C	23	GENIC	homozygous	114541474
13	41908576	41908577	T	G	13	GENIC	homozygous	114541476
13	41916415	41916416	T	G	3	GENIC	homozygous	114329968
13	41916418	41916419	C	T	3	GENIC	homozygous	114329970
13	41916419	41916420	A	G	2	GENIC	homozygous	114329972
13	41916425	41916426	C	G	2	GENIC	homozygous	114329974
13	41920229	41920230	A	G	21	GENIC	homozygous	114541498
13	41916428	41916429	C	T	1	GENIC	homozygous	114665166