chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24482977	24482978	G	A	29	GENIC	homozygous	115422237
12	24484138	24484139	G	A	8	GENIC	heterozygous	115510232
12	24484139	24484140	C	T	9	GENIC	heterozygous	115510233
12	24484142	24484143	G	A	9	GENIC	heterozygous	115510234
12	24484143	24484144	C	T	9	GENIC	heterozygous	115510235
12	24484145	24484146	C	T	9	GENIC	heterozygous	115510236
12	24484148	24484149	G	A	9	GENIC	heterozygous	115510237
12	24484149	24484150	A	T	9	GENIC	heterozygous	115510238
12	24488302	24488303	A	G	21	GENIC	homozygous	115288004
12	24493307	24493308	A	G	28	GENIC	homozygous	115288022
12	24493416	24493417	C	T	22	GENIC	homozygous	115288024
12	24493624	24493625	A	G	31	GENIC	homozygous	115288026
12	24493840	24493841	A	G	7	GENIC	homozygous	115510239
12	24499322	24499323	T	C	19	GENIC	homozygous	115288058
12	24501293	24501294	G	A	21	GENIC	homozygous	115288070
12	24517790	24517791	A	G	23	GENIC	homozygous	115288140
12	24521733	24521734	T	C	41	GENIC	homozygous	115422243
12	24526795	24526796	T	C	21	GENIC	homozygous	115288184
12	24527565	24527566	C	T	13	GENIC	heterozygous	115510240
12	24530944	24530945	T	A	18	GENIC	homozygous	115288208
12	24534997	24534998	T	C	22	GENIC	homozygous	115422245