chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	40742723	40742724	T	C	49	GENIC	homozygous	116570313
10	40743302	40743303	T		32	GENIC	possibly homozygous	128810105
10	40743859	40743860	C	T	41	GENIC	homozygous	116570315
10	40744007	40744008	T	C	46	GENIC	homozygous	116570319
10	40744265	40744266	C	T	58	GENIC	homozygous	116764658
10	40744297	40744298	A	G	57	GENIC	homozygous	116764660
10	40744405	40744406	T		56	GENIC	homozygous	131091762
10	40743993	40743993		A	45	GENIC	homozygous	131091759
10	40744280	40744282	AC		53	GENIC	homozygous	131091760
10	40744402	40744404	CG		56	GENIC	homozygous	131091761
10	40747091	40747092	T	C	56	GENIC	homozygous	116764672
10	40748128	40748129	A	G	54	GENIC	possibly homozygous	116570323
10	40748562	40748563	T	C	50	GENIC	possibly homozygous	116764682
10	40745948	40745949	A	C	39	GENIC	homozygous	116870800
10	40746784	40746785	G	A	47	GENIC	homozygous	116870802
10	40748363	40748364	G	C	52	GENIC	homozygous	116870804
10	40751233	40751234	A		58	GENIC	homozygous	128810107
10	40751282	40751283	G	A	59	GENIC	homozygous	116570337
10	40751355	40751356	G	A	50	GENIC	homozygous	116870806
10	40752102	40752103	T	C	66	GENIC	homozygous	116870808
10	40752235	40752236	C	T	58	GENIC	homozygous	116870810
10	40752356	40752368	CTACTGCTGAAG		56	GENIC	homozygous	131091763
10	40755326	40755327	G	A	43	GENIC	homozygous	116870812
10	40755514	40755515	T	C	42	GENIC	homozygous	116870814
10	40755828	40755829	A	G	51	GENIC	homozygous	116870816
10	40756811	40756812	T	C	59	GENIC	homozygous	116570357
10	40756863	40756864	C	T	59	GENIC	homozygous	116870818
10	40758542	40758543	C	T	40	GENIC	homozygous	116870820
10	40758944	40758945	G	A	50	GENIC	homozygous	116870822
10	40760334	40760335	G	A	25	GENIC	homozygous	117076640
10	40762747	40762748	G	A	58	GENIC	homozygous	116870824