chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	61477979	61477980	C	T	34	GENIC	homozygous	51470881
10	61478397	61478398	C	A	34	GENIC	homozygous	51670531
10	61479402	61479403	C	-	15	GENIC	homozygous	51670534
10	61480225	61480226	G	A	37	GENIC	homozygous	51670536
10	61481485	61481486	A	-	25	GENIC	homozygous	51670538
10	61482529	61482530	C	T	6	GENIC	homozygous	51470883
10	61484739	61484740	T	TA	2	GENIC	heterozygous	51470884
10	61484744	61484745	A	AT	13	GENIC	homozygous	51470885
10	61484745	61484746	A	AT	14	GENIC	homozygous	51670540
10	61486449	61486450	T	TA	14	GENIC	possibly homozygous	51670542
10	61487708	61487709	G	A	25	GENIC	homozygous	51670544
10	61488757	61488758	C	T	24	GENIC	homozygous	51670546
10	61490327	61490328	G	C	41	GENIC	homozygous	51670548
10	61490420	61490421	T	TTC	17	GENIC	heterozygous	51670550
10	61490957	61490958	G	A	31	GENIC	homozygous	51670552
10	61491336	61491337	G	GC	18	GENIC	homozygous	51670554
10	61492517	61492518	A	C	18	GENIC	homozygous	51670556