chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	7659151	7659152	C	A	34	GENIC	possibly homozygous	108040008
1	7659218	7659219	A	G	16	GENIC	homozygous	108040009
1	7659224	7659225	A	G	13	GENIC	homozygous	108040010
1	7659468	7659469	A	C	46	GENIC	homozygous	108040012
1	7661127	7661128	C	T	45	GENIC	homozygous	108826334
1	7661232	7661233	A	C	62	GENIC	homozygous	108040024
1	7661640	7661641	T	C	38	GENIC	homozygous	108040026
1	7662567	7662568	T	C	52	GENIC	homozygous	108040027
1	7662641	7662642	G	A	70	GENIC	possibly homozygous	108826335
1	7662792	7662793	G	A	52	GENIC	homozygous	108826336
1	7663088	7663089	A	G	48	GENIC	homozygous	108826337
1	7664416	7664417	T	A	57	GENIC	homozygous	108040030
1	7664426	7664427	G	T	58	GENIC	possibly homozygous	108040031
1	7665244	7665245	T	C	56	GENIC	homozygous	108826338
1	7665306	7665307	G	T	50	GENIC	possibly homozygous	108826339
1	7665741	7665742	G	A	46	GENIC	homozygous	108826340
1	7665767	7665768	T	C	51	GENIC	homozygous	108040034
1	7667070	7667071	G	A	34	GENIC	homozygous	108826341
1	7667180	7667181	C	T	57	GENIC	homozygous	108826342
1	7667394	7667395	C	A	58	GENIC	homozygous	108826343
1	7668560	7668561	A	C	42	GENIC	homozygous	108826344
1	7669703	7669704	T	C	34	GENIC	homozygous	108826345
1	7669877	7669878	T	C	51	GENIC	homozygous	108826346
1	7669954	7669955	T	C	52	GENIC	homozygous	108040037
1	7670184	7670185	G	T	50	GENIC	possibly homozygous	108826347
1	7670337	7670338	T	G	46	GENIC	homozygous	108040038
1	7671340	7671341	T	C	69	GENIC	homozygous	108826348
1	7671774	7671775	A	G	49	GENIC	homozygous	108040039
1	7671983	7671984	T	G	44	GENIC	heterozygous	109468733
1	7672587	7672588	T	C	59	GENIC	homozygous	108040042
1	7673068	7673069	T	C	44	GENIC	homozygous	108040043
1	7673233	7673234	A	G	67	GENIC	homozygous	108040044
1	7673517	7673518	C	T	40	GENIC	homozygous	108826349