chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	59104175	59104176	C	T	38	GENIC	possibly homozygous	73634938
2	59105961	59105962	G	A	37	GENIC	homozygous	73634941
2	59107589	59107590	C	T	17	GENIC	homozygous	73634944
2	59107906	59107907	G	T	27	GENIC	homozygous	73634947
2	59107910	59107911	C	T	25	GENIC	homozygous	73634950
2	59109171	59109172	A	T	24	GENIC	homozygous	73634953
2	59109719	59109720	G	A	35	GENIC	homozygous	73634956
2	59110564	59110565	C	G	16	GENIC	homozygous	73634959
2	59110604	59110605	G	A	25	GENIC	homozygous	73634962
2	59110944	59110945	C	G	38	GENIC	homozygous	73634965
2	59111171	59111172	A	G	10	GENIC	homozygous	73634971
2	59111426	59111427	G	A	22	GENIC	homozygous	73634974
2	59111610	59111611	C	T	14	GENIC	homozygous	73634977
2	59111741	59111742	A	C	20	GENIC	homozygous	73634980
2	59111943	59111944	G	A	9	GENIC	possibly homozygous	73634986
2	59111999	59112000	T	C	17	GENIC	homozygous	73634992
2	59112082	59112083	A	G	11	GENIC	homozygous	73634995
2	59112303	59112304	C	T	33	GENIC	homozygous	73634998
2	59113470	59113471	C	A	27	GENIC	homozygous	73635001
2	59113803	59113804	G	A	39	GENIC	homozygous	73635004
2	59114582	59114583	C	T	38	GENIC	homozygous	73635007
2	59114681	59114682	A	G	27	GENIC	homozygous	73635010
2	59115145	59115146	A	T	34	GENIC	homozygous	73635013
2	59115269	59115270	T	C	46	GENIC	homozygous	73635016
2	59115291	59115292	C	A	44	GENIC	homozygous	73635019
2	59115480	59115481	A	G	18	GENIC	homozygous	73635022
2	59116110	59116111	C	T	22	GENIC	homozygous	73635025
2	59116807	59116808	C	T	14	GENIC	homozygous	73635028
2	59117144	59117145	C	A	20	GENIC	homozygous	73635031
2	59118739	59118740	A	C	33	GENIC	homozygous	73635034
2	59121466	59121467	A	G	22	GENIC	homozygous	73635037
2	59124044	59124045	C	T	12	GENIC	homozygous	73635043
2	59125151	59125152	G	A	28	GENIC	homozygous	73635046
2	59126024	59126025	T	C	16	GENIC	homozygous	73635049
2	59127157	59127158	G	A	30	GENIC	homozygous	73635061