chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	30104055	30104056	C	T	35	GENIC	homozygous	116752025
10	30104878	30104879	A	C	36	GENIC	homozygous	116542457
10	30106075	30106076	G	C	28	GENIC	homozygous	116542461
10	30106402	30106403	A	G	36	GENIC	homozygous	116752027
10	30106607	30106608	G	A	32	GENIC	homozygous	116752029
10	30107214	30107215	A	G	37	GENIC	homozygous	116752031
10	30107322	30107323	A	G	37	GENIC	homozygous	116542467
10	30107554	30107555	G	A	39	GENIC	homozygous	116542471
10	30108374	30108375	A	T	37	GENIC	homozygous	116752033
10	30108584	30108585	T	C	30	GENIC	homozygous	116542473
10	30109371	30109372	C	T	22	GENIC	homozygous	116752035
10	30110044	30110045	A	T	28	GENIC	homozygous	116752037
10	30110281	30110282	C	G	11	GENIC	homozygous	116542475
10	30111069	30111070	A	G	38	GENIC	homozygous	116752039
10	30111284	30111285	C	G	20	GENIC	homozygous	116752041
10	30114462	30114463	A	T	27	GENIC	homozygous	116752043
10	30114475	30114476	T	G	24	GENIC	homozygous	116542481
10	30116108	30116109	T	C	33	GENIC	possibly homozygous	116542483
10	30116898	30116899	C	G	42	GENIC	homozygous	116752045