chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	66226355	66226356	G	A	43	GENIC	homozygous	118068108
10	66226424	66226425	T	C	46	GENIC	homozygous	117219761
10	66226431	66226432	C	T	43	GENIC	homozygous	118068109
10	66226484	66226485	T	G	40	GENIC	homozygous	116942363
10	66226493	66226494	G	T	41	GENIC	homozygous	116942365
10	66226639	66226640	T	C	39	GENIC	homozygous	116793819
10	66226771	66226772	C	A	42	GENIC	homozygous	116942367
10	66227328	66227329	T	C	38	GENIC	homozygous	117411507
10	66227483	66227484	A	G	39	GENIC	homozygous	118041761
10	66227484	66227485	G	C	39	GENIC	homozygous	118041762
10	66228018	66228019	C	G	35	GENIC	possibly homozygous	118041772
10	66228087	66228088	G	A	24	GENIC	possibly homozygous	117998830
10	66228119	66228120	T	C	25	GENIC	possibly homozygous	117998831
10	66228196	66228197	G	C	35	GENIC	homozygous	117998832
10	66228265	66228266	A	C	44	GENIC	homozygous	123375298
10	66228267	66228268	A	T	43	GENIC	homozygous	117219763
10	66228278	66228279	T	A	45	GENIC	homozygous	117998833
10	66228378	66228379	C	A	42	GENIC	possibly homozygous	117219765
10	66228431	66228432	T	G	25	GENIC	possibly homozygous	118041774
10	66228476	66228477	G	A	13	GENIC	homozygous	117998834
10	66228511	66228512	C	G	15	GENIC	homozygous	117998835
10	66228605	66228606	C	A	45	GENIC	homozygous	118068110
10	66228639	66228640	C	T	54	GENIC	homozygous	117998836
10	66228758	66228759	A	G	41	GENIC	homozygous	117998838
10	66228768	66228769	T	C	46	GENIC	homozygous	117411509
10	66228769	66228770	G	A	44	GENIC	homozygous	117411511
10	66228877	66228878	C	T	63	GENIC	homozygous	118068111
10	66229037	66229038	A	G	43	GENIC	homozygous	116793821
10	66229069	66229070	G	T	39	GENIC	homozygous	116793825
10	66229091	66229092	C	T	35	GENIC	homozygous	116793827
10	66229196	66229197	C	T	41	GENIC	homozygous	116942369
10	66229238	66229239	G	T	47	GENIC	homozygous	116793829
10	66228760	66228761	C	A	43	GENIC	homozygous	116620162
10	66227211	66227212	T		25	GENIC	homozygous	131708456
10	66227213	66227329	CCATCATGTTAAAGCTTCCTGACCCAGGGACACCGCTAACACTCATAACGCACTGTCTGAGCACCAGGCTAAGACATCACGCTATATGCGGTCACCGCCCAGAGTGTGCTGCAGAT		38	GENIC	heterozygous	131708457
10	66227053	66227053		A	40	GENIC	homozygous	128826176
10	66228237	66228241	AAGG		41	GENIC	homozygous	128826177
10	66228266	66228267	G	T	44	GENIC	homozygous	118084188
10	66228453	66228454	G	A	22	GENIC	possibly homozygous	118084189
10	66228284	66228285	C	T	46	GENIC	homozygous	117196331
10	66228394	66228398	AAAC		31	GENIC	possibly homozygous	131465891
10	66228596	66228596		G	41	GENIC	homozygous	131465892