chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59831972	59831973	C	T	34	GENIC	homozygous	116608864
10	59846814	59846815	C	T	19	GENIC	homozygous	116937922
10	59835209	59835210	T	C	26	GENIC	homozygous	116937912
10	59840287	59840288	G	A	30	GENIC	homozygous	116937914
10	59840802	59840803	C	T	28	GENIC	homozygous	116937916
10	59841913	59841914	C	T	27	GENIC	homozygous	116937918
10	59845872	59845873	G	A	23	GENIC	homozygous	116937920
10	59847075	59847076	C	T	21	GENIC	homozygous	116937924
10	59850533	59850534	T	C	23	GENIC	homozygous	116608906
10	59851271	59851272	G	A	25	GENIC	homozygous	116937926
10	59852336	59852337	G	A	21	GENIC	homozygous	116937928
10	59853841	59853842	C	A	31	GENIC	homozygous	116937930
10	59854673	59854674	T	C	12	GENIC	homozygous	116608908
10	59854980	59854981	T	C	31	GENIC	homozygous	116937932
10	59856557	59856558	C	T	31	GENIC	homozygous	116937934
10	59857724	59857725	T	C	34	GENIC	homozygous	116937942
10	59856817	59856818	G	A	28	GENIC	homozygous	116937936
10	59856976	59856977	G	T	29	GENIC	homozygous	116937938
10	59857572	59857573	G	A	22	GENIC	homozygous	116937940
10	59857784	59857785	T	A	28	GENIC	homozygous	116937944
10	59858183	59858184	C	T	19	GENIC	homozygous	116937946
10	59859639	59859640	A	T	22	GENIC	homozygous	116937948
10	59859946	59859947	C	T	27	GENIC	homozygous	116937950
10	59860050	59860051	G	T	20	GENIC	homozygous	116608910
10	59860250	59860251	C	T	27	GENIC	homozygous	116937952
10	59860789	59860790	C	T	20	GENIC	homozygous	116937954
10	59863324	59863325	A	G	18	GENIC	homozygous	116937956
10	59863574	59863575	G	A	27	GENIC	homozygous	116937958