chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13061582	13061583	A		6	GENIC	heterozygous	133635113
10	13061622	13061623	A	G	14	GENIC	homozygous	116975829
10	13067005	13067006	T	C	19	GENIC	homozygous	117982113
10	13067069	13067070	G	A	21	GENIC	homozygous	118029980
10	13070473	13070474	C	G	43	GENIC	homozygous	116735585
10	13066097	13066098	G	T	12	GENIC	possibly homozygous	116735578
10	13066407	13066408	T	C	22	GENIC	homozygous	116735579
10	13067363	13067364	A	G	29	GENIC	homozygous	116735580
10	13067593	13067594	G	A	43	GENIC	homozygous	116735581
10	13068427	13068428	C	A	19	GENIC	homozygous	116735582
10	13069261	13069262	T	A	39	GENIC	homozygous	116735583
10	13070204	13070205	G	C	30	GENIC	homozygous	116735584
10	13066747	13066748	T	G	31	GENIC	homozygous	117120327
10	13070495	13070496	T	C	41	GENIC	homozygous	116735586
10	13070588	13070589	A	G	38	GENIC	homozygous	116735587
10	13071530	13071531	G	A	34	GENIC	homozygous	116735588
10	13071760	13071761	T	C	39	GENIC	homozygous	116735589