chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59897787	59897788	A	G	59	GENIC	homozygous	116608928
10	59899171	59899172	A	G	19	GENIC	homozygous	116789015
10	59899182	59899183	A	G	21	GENIC	homozygous	116789017
10	59899632	59899633	A	G	39	GENIC	homozygous	117995668
10	59899340	59899340		A	35	GENIC	homozygous	128820949
10	59899537	59899538	G	T	40	GENIC	homozygous	117995664
10	59899555	59899556	G	A	39	GENIC	homozygous	117995665
10	59899594	59899595	T	C	36	GENIC	homozygous	117995666
10	59899631	59899632	C	T	36	GENIC	homozygous	117995667
10	59899636	59899637	A	G	37	GENIC	homozygous	116608930
10	59899647	59899648	C	T	36	GENIC	homozygous	117142509
10	59899677	59899678	T	C	30	GENIC	homozygous	116608932
10	59900119	59900120	G	A	40	GENIC	homozygous	116608936
10	59901862	59901862		TGCA	20	GENIC	homozygous	131095240
10	59900321	59900322	T	G	44	GENIC	homozygous	116608938
10	59901872	59901873	G	T	20	GENIC	homozygous	123366670
10	59902484	59902485	C	T	50	GENIC	homozygous	116608940
10	59902978	59902979	T	C	43	GENIC	homozygous	116608942
10	59903020	59903021	T	C	54	GENIC	homozygous	116608944
10	59905945	59905946	C	T	34	GENIC	homozygous	116789019
10	59909658	59909659	T	C	26	GENIC	homozygous	116608946
10	59901864	59901864		G	20	GENIC	homozygous	131095241
10	59901867	59901867		TGCA	20	GENIC	homozygous	131095242