chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	74666052	74666053	T	A	12	GENIC	homozygous	58889194
2	74666392	74666393	G	T	3	GENIC	homozygous	61709277
2	74667219	74667220	G	A	23	GENIC	homozygous	61709279
2	74667230	74667231	C	CAT	23	GENIC	homozygous	61709281
2	74667706	74667707	G	A	34	GENIC	homozygous	61709283
2	74667953	74667954	T	A	26	GENIC	homozygous	61709285
2	74668219	74668220	C	T	24	GENIC	homozygous	61709287
2	74668325	74668326	C	T	41	GENIC	homozygous	61709289
2	74668344	74668345	G	C	42	GENIC	homozygous	61709291
2	74668345	74668346	C	A	40	GENIC	homozygous	61709293
2	74668907	74668908	A	G	17	GENIC	homozygous	61709295
2	74669081	74669082	T	C	16	GENIC	homozygous	61709298
2	74669214	74669215	A	T	16	GENIC	homozygous	58889197
2	74669217	74669218	C	T	16	GENIC	homozygous	58889198
2	74669330	74669331	C	G	27	GENIC	homozygous	61709300
2	74669419	74669420	G	C	22	GENIC	homozygous	61709302
2	74669743	74669744	A	G	26	GENIC	homozygous	61709304
2	74669852	74669853	T	C	28	GENIC	homozygous	61709306
2	74670089	74670090	T	G	18	GENIC	homozygous	61709308
2	74671519	74671520	A	C	11	GENIC	homozygous	60446031
2	74671965	74671966	C	T	15	GENIC	homozygous	61709310