chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59110870	59110871	A	C	24	GENIC	homozygous	117108083
8	59111831	59111832	G	A	34	GENIC	homozygous	117184656
8	59111946	59111947	G	T	25	GENIC	homozygous	116510932
8	59111951	59111952	T	C	26	GENIC	homozygous	116510934
8	59112336	59112337	G	A	25	GENIC	homozygous	117184657
8	59112454	59112455	C	T	17	GENIC	homozygous	117184658
8	59112618	59112619	G	A	22	GENIC	homozygous	116510938
8	59113093	59113094	C	T	35	GENIC	homozygous	116510940
8	59113206	59113207	C	G	37	GENIC	homozygous	116510942
8	59113516	59113517	C	T	18	GENIC	homozygous	116510944
8	59113562	59113563	A	G	22	GENIC	homozygous	116510946
8	59113757	59113758	T	G	36	GENIC	homozygous	116510950
8	59115954	59115955	C	T	23	GENIC	homozygous	117184660
8	59116116	59116117	A	G	23	GENIC	homozygous	116510962
8	59116629	59116630	C	T	26	GENIC	homozygous	117184661
8	59116741	59116742	A	T	43	GENIC	homozygous	116510966
8	59117157	59117158	C	T	24	GENIC	homozygous	116510969
8	59117216	59117217	C	T	29	GENIC	homozygous	116510971
8	59117305	59117306	C	T	24	GENIC	possibly homozygous	116510973
8	59117945	59117946	G	A	28	GENIC	homozygous	116510977
8	59118083	59118084	C	T	39	GENIC	homozygous	117184662
8	59118542	59118543	C	T	33	GENIC	homozygous	117184664
8	59119213	59119214	G	A	22	GENIC	homozygous	116511015
8	59119449	59119450	A	G	26	GENIC	homozygous	116511017
8	59119608	59119609	C	T	43	GENIC	homozygous	116511019
8	59119760	59119761	C	G	25	GENIC	homozygous	116511021
8	59119878	59119879	C	T	23	GENIC	homozygous	116511023
8	59121107	59121108	G	A	24	GENIC	homozygous	116511035
8	59121238	59121239	C	G	33	GENIC	homozygous	116511037
8	59121566	59121567	A	G	27	GENIC	homozygous	116511039
8	59121826	59121827	C	T	34	GENIC	homozygous	116511041
8	59121882	59121883	G	A	45	GENIC	homozygous	116511043
8	59122316	59122317	C	T	26	GENIC	homozygous	116511045
8	59122543	59122544	T	C	28	GENIC	homozygous	116511049
8	59122697	59122698	T	A	30	GENIC	homozygous	116511051