chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	76152613	76152614	G	T	7	GENIC	heterozygous	117391707
10	76153557	76153558	C	T	25	GENIC	homozygous	116801090
10	76155092	76155093	G	A	15	GENIC	homozygous	116640753
10	76156530	76156531	A	G	14	GENIC	homozygous	116640757
10	76156619	76156620	C	A	22	GENIC	homozygous	116640759
10	76156686	76156687	A	G	22	GENIC	homozygous	116640761
10	76156733	76156734	T	C	21	GENIC	homozygous	116640763
10	76162083	76162084	T	G	23	GENIC	homozygous	116801092
10	76162817	76162818	A	G	13	GENIC	homozygous	116640769
10	76166234	76166235	A	G	24	GENIC	homozygous	116640779
10	76167350	76167351	T	A	30	GENIC	homozygous	116801094
10	76168162	76168163	A	G	24	GENIC	homozygous	116640783
10	76168515	76168516	T	A	23	GENIC	homozygous	116801096
10	76169175	76169176	G	A	25	GENIC	homozygous	116801098
10	76171667	76171668	T	C	19	GENIC	homozygous	116640789
10	76177115	76177116	G	A	22	GENIC	homozygous	116801100
10	76178024	76178025	A	G	27	GENIC	homozygous	116640809
10	76178455	76178456	T	C	27	GENIC	homozygous	116640813
10	76180765	76180766	A	G	24	GENIC	homozygous	116640815
10	76181507	76181508	A	C	20	GENIC	homozygous	116640819
10	76181858	76181859	A	G	18	GENIC	homozygous	116640821
10	76182425	76182426	G	A	25	GENIC	homozygous	116801104
10	76182710	76182711	C	T	24	GENIC	homozygous	116801106
10	76182798	76182799	A	G	19	GENIC	homozygous	116801108