chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	61477979	61477980	C	T	26	GENIC	homozygous	51470881
10	61478397	61478398	C	A	35	GENIC	homozygous	51670531
10	61479402	61479403	C	-	20	GENIC	homozygous	51670534
10	61480225	61480226	G	A	40	GENIC	homozygous	51670536
10	61481485	61481486	A	-	25	GENIC	homozygous	51670538
10	61484744	61484745	A	AT	16	GENIC	homozygous	51470885
10	61484745	61484746	A	AT	16	GENIC	homozygous	51670540
10	61486285	61486286	G	GTT	13	GENIC	homozygous	52379981
10	61486449	61486450	T	TA	26	GENIC	homozygous	51670542
10	61487708	61487709	G	A	35	GENIC	homozygous	51670544
10	61488757	61488758	C	T	26	GENIC	homozygous	51670546
10	61490327	61490328	G	C	32	GENIC	homozygous	51670548
10	61490420	61490421	T	TTC	6	GENIC	homozygous	51670550
10	61490957	61490958	G	A	26	GENIC	homozygous	51670552
10	61491336	61491337	G	GC	33	GENIC	homozygous	51670554