chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13914066	13914067	C	T	23	GENIC	homozygous	116736542
10	13914454	13914455	T	C	32	GENIC	homozygous	116736543
10	13914516	13914517	T	G	16	GENIC	homozygous	116736544
10	13917401	13917402	G	A	48	GENIC	homozygous	116736545
10	13919181	13919182	A	C	6	GENIC	homozygous	117074882
10	13920131	13920132	C	A	34	GENIC	homozygous	116736547
10	13921816	13921817	T	C	37	GENIC	homozygous	116736548
10	13922436	13922437	G	A	20	GENIC	homozygous	116736549
10	13923904	13923905	T	C	50	GENIC	homozygous	116736550
10	13926199	13926200	A	T	38	GENIC	homozygous	116736551
10	13926356	13926357	C	T	32	GENIC	homozygous	116736552
10	13931009	13931010	T	C	34	GENIC	homozygous	116736553
10	13934783	13934784	A	G	17	GENIC	homozygous	116736554
10	13935389	13935390	A	G	26	GENIC	homozygous	116736555
10	13935572	13935573	G	A	29	GENIC	homozygous	116736556
10	13938869	13938870	T	C	28	GENIC	homozygous	116736557
10	13941160	13941161	A	G	37	GENIC	homozygous	116736558
10	13947890	13947891	A	G	29	GENIC	homozygous	116736559
10	13948000	13948001	T	C	26	GENIC	homozygous	116736560
10	13948007	13948008	A	C	24	GENIC	homozygous	116736561
10	13951426	13951427	A	G	20	GENIC	homozygous	116736563
10	13956996	13956997	T	C	13	GENIC	homozygous	116736564
10	13957869	13957870	G	C	33	GENIC	homozygous	116736565