chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109707884	109707885	T	C	39	GENIC	homozygous	116983819
10	109707985	109707996	CGCTCGAGGAC		68	GENIC	homozygous	132148046
10	109712254	109712254		T	67	GENIC	homozygous	132148047
10	109712825	109712825		CACACACACACA	20	GENIC	homozygous	132148048
10	109711454	109711455	A	G	55	GENIC	homozygous	116719021
10	109708375	109708376	G	A	62	GENIC	homozygous	116909707
10	109708616	109708617	A	G	71	GENIC	possibly homozygous	116909709
10	109710993	109710994	C	A	53	GENIC	homozygous	116909710
10	109712255	109712256	A	C	66	GENIC	homozygous	116909711
10	109714738	109714738		CTGGGCTGTGGGTCAGGTTGCCCATTCTTGGCTGAATGC	69	GENIC	homozygous	132148049
10	109714779	109714780	C	T	72	GENIC	homozygous	116909712
10	109716180	109716181	A	T	83	GENIC	homozygous	116961940
10	109715206	109715207	C	T	62	GENIC	homozygous	116909713
10	109714734	109714735	T	C	67	GENIC	homozygous	117072051