chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97190846	97190847	G	A	16	GENIC	homozygous	51556326
10	97191450	97191451	G	A	7	GENIC	homozygous	51556327
10	97191733	97191734	T	TG	9	GENIC	homozygous	51556328
10	97191950	97191951	C	T	13	GENIC	homozygous	51556329
10	97192217	97192218	C	T	12	GENIC	homozygous	51556330
10	97192413	97192414	C	T	17	GENIC	homozygous	51556331
10	97192670	97192671	G	GCCT	10	GENIC	homozygous	51556332
10	97193350	97193351	G	A	6	GENIC	homozygous	51556333
10	97194155	97194156	G	A	18	GENIC	homozygous	51556341
10	97194576	97194578	AA	--	9	GENIC	possibly homozygous	52811659
10	97194593	97194594	A	G	4	GENIC	homozygous	51556347
10	97194597	97194598	A	G	4	GENIC	homozygous	52811662
10	97194601	97194602	A	G	3	GENIC	homozygous	52811665
10	97194605	97194606	A	G	1	GENIC	homozygous	53170205
10	97194628	97194629	A	AGAAAAGAAAGAT	4	GENIC	heterozygous	52767140
10	97196956	97196957	G	A	15	GENIC	homozygous	51556349
10	97196996	97197003	CCCCGTT	-------	17	GENIC	homozygous	51556350
10	97197055	97197056	C	T	23	GENIC	homozygous	51556351
10	97197176	97197177	C	G	13	GENIC	homozygous	51556352
10	97197246	97197247	A	T	11	GENIC	homozygous	51556353
10	97197458	97197459	A	G	12	GENIC	homozygous	51556354
10	97197728	97197729	C	G	12	GENIC	homozygous	51556355
10	97198406	97198413	AGAAAAG	-------	21	GENIC	homozygous	51556356
10	97198461	97198462	C	CG	16	GENIC	possibly homozygous	51556357
10	97199457	97199458	C	CA	17	GENIC	homozygous	51556358
10	97199777	97199778	G	A	21	GENIC	homozygous	51556359