chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	166490714	166490721	GTTTTTT	-------	3	GENIC	homozygous	56363442
5	166491301	166491302	C	G	15	GENIC	homozygous	56079258
5	166491858	166491859	C	-	6	GENIC	heterozygous	56363443
5	166496076	166496077	A	G	10	GENIC	possibly homozygous	56363444
5	166497752	166497753	A	G	32	GENIC	possibly homozygous	56363445
5	166497909	166497910	G	A	11	GENIC	homozygous	56363446
5	166499143	166499144	A	G	20	GENIC	possibly homozygous	56079286
5	166499317	166499318	T	C	9	GENIC	homozygous	56079290
5	166500167	166500168	G	A	18	GENIC	possibly homozygous	56079292
5	166501166	166501167	A	G	8	GENIC	possibly homozygous	56079295
5	166501184	166501185	A	G	7	GENIC	homozygous	56363447
5	166501185	166501186	A	C	7	GENIC	homozygous	56363448
5	166501228	166501229	G	-	9	GENIC	homozygous	56363449
5	166502033	166502034	A	C	19	GENIC	homozygous	56079296
5	166502492	166502493	T	C	18	GENIC	homozygous	56363450
5	166502815	166502816	C	CAT	7	GENIC	homozygous	56363451
5	166503649	166503653	ACAG	----	6	GENIC	heterozygous	56363452
5	166503763	166503764	T	C	14	GENIC	homozygous	56079305
5	166504047	166504048	A	G	20	GENIC	homozygous	56079307
5	166504153	166504154	G	A	19	GENIC	homozygous	56079308
5	166506774	166506775	T	G	24	GENIC	possibly homozygous	56079317
5	166507520	166507521	A	C	17	GENIC	possibly homozygous	56079319
5	166508154	166508155	G	GC	13	GENIC	possibly homozygous	56363453
5	166509681	166509682	A	G	16	GENIC	possibly homozygous	56079324
5	166510443	166510444	G	GC	21	GENIC	homozygous	56079327
5	166512058	166512059	A	G	20	GENIC	homozygous	56363454
5	166512877	166512878	C	T	22	GENIC	homozygous	56363455
5	166515305	166515306	A	G	23	GENIC	homozygous	56363456
5	166517849	166517850	C	T	6	GENIC	homozygous	56363457
5	166521784	166521788	TTCT	----	1	GENIC	homozygous	56079340