chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59013706	59013707	C	T	36	GENIC	homozygous	116937388
10	59014631	59014632	A	C	32	GENIC	homozygous	116937390
10	59014989	59014990	T	C	40	GENIC	homozygous	116607644
10	59015356	59015357	C	T	28	GENIC	homozygous	116937392
10	59017170	59017171	T	C	34	GENIC	homozygous	116937394
10	59017660	59017661	C	T	32	GENIC	homozygous	116937396
10	59018343	59018344	T	C	28	GENIC	homozygous	116937398
10	59018698	59018699	G	A	30	GENIC	homozygous	116937400
10	59020521	59020522	T	C	11	GENIC	possibly homozygous	117130816
10	59021211	59021212	T	C	25	GENIC	homozygous	116788218
10	59021242	59021243	G	A	23	GENIC	homozygous	116937402
10	59022323	59022324	A	G	43	GENIC	homozygous	116607646
10	59023214	59023215	G	A	33	GENIC	homozygous	116937404
10	59027609	59027610	A	G	30	GENIC	homozygous	116788228
10	59038643	59038644	C	T	26	GENIC	homozygous	116788232
10	59041298	59041299	C	G	31	GENIC	homozygous	116937408
10	59041309	59041310	C	A	32	GENIC	possibly homozygous	116937410
10	59046253	59046254	G	A	21	GENIC	homozygous	116937412