chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	167673011	167673012	C	T	28	GENIC	homozygous	114455428
5	167673282	167673283	T	A	31	GENIC	homozygous	114455429
5	167674572	167674573	A	T	13	GENIC	homozygous	114455430
5	167675566	167675567	A	G	24	GENIC	homozygous	114455431
5	167677103	167677104	C	A	26	GENIC	homozygous	114455432
5	167677146	167677147	T	C	31	GENIC	homozygous	114455433
5	167677227	167677228	G	A	28	GENIC	homozygous	114455434
5	167677396	167677397	G	A	27	GENIC	homozygous	114455435
5	167677563	167677564	A	G	16	GENIC	possibly homozygous	114455436
5	167678776	167678777	C	T	23	GENIC	heterozygous	114455437
5	167678780	167678781	C	T	23	GENIC	heterozygous	114455438
5	167679585	167679586	G	A	25	GENIC	homozygous	114455439
5	167680482	167680483	T	C	29	GENIC	heterozygous	114162879
5	167684881	167684882	A	G	26	GENIC	homozygous	114082563
5	167685112	167685113	G	T	16	GENIC	homozygous	114082565
5	167685511	167685512	T	A	53	GENIC	heterozygous	114082567
5	167686011	167686012	T	C	22	GENIC	heterozygous	114604606
5	167691475	167691476	C	A	16	GENIC	homozygous	114361060
5	167693901	167693902	G	T	12	GENIC	homozygous	114082597
5	167694282	167694283	C	T	16	GENIC	homozygous	114082600
5	167694395	167694396	A	T	26	GENIC	homozygous	114082602
5	167694456	167694457	G	A	13	GENIC	homozygous	114082603
5	167694841	167694842	T	A	11	GENIC	homozygous	114082605
5	167695429	167695430	A	C	22	GENIC	homozygous	114455440