chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	95700407	95700408	A	G	28	GENIC	homozygous	61478120
1	95700512	95700513	C	-	18	GENIC	homozygous	61952513
1	95700922	95700923	T	C	33	GENIC	homozygous	61952514
1	95701166	95701167	T	G	41	GENIC	homozygous	61952515
1	95702351	95702352	T	C	29	GENIC	homozygous	61478123
1	95703188	95703189	T	TTTTTTG	18	GENIC	homozygous	61478125
1	95703908	95703909	A	G	17	GENIC	homozygous	61478126
1	95704068	95704069	T	G	28	GENIC	homozygous	61478128
1	95704343	95704344	G	GAC	9	GENIC	homozygous	61478129
1	95704371	95704372	G	GAC	10	GENIC	homozygous	61478130
1	95704447	95704448	C	T	9	GENIC	homozygous	61478131
1	95705252	95705253	A	G	26	GENIC	homozygous	61478134
1	95705456	95705457	G	A	24	GENIC	homozygous	61478135
1	95705763	95705764	A	G	15	GENIC	homozygous	61478136
1	95705948	95705949	C	G	21	GENIC	homozygous	61952516
1	95706485	95706486	T	C	29	GENIC	homozygous	61478138
1	95703411	95703413	AA	--	21	GENIC	possibly homozygous	62016470
1	95704285	95704286	G	GACAC	3	GENIC	homozygous	62144338
1	95706257	95706258	A	AC	27	GENIC	homozygous	62144339
1	95706258	95706259	A	AAACAAAC	26	GENIC	homozygous	62144341
1	95707033	95707034	A	ACTGCGGAGAACCCTTCCCGGACTCACAGCTCGCACACAACCCTGAGACTCAGTGGCCCTAGCGTTC	25	GENIC	homozygous	62144343