chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91186168	91186169	C	G	42	GENIC	homozygous	116951788
10	91186938	91186939	A	G	60	GENIC	possibly homozygous	116821825
10	91187612	91187613	C	G	55	GENIC	homozygous	116821827
10	91187613	91187614	C	T	54	GENIC	homozygous	116821829
10	91187653	91187654	A	G	54	GENIC	homozygous	116821831
10	91187792	91187793	A	G	53	GENIC	homozygous	116821833
10	91189741	91189742	A	C	56	GENIC	homozygous	116821835
10	91190326	91190327	A	G	54	GENIC	possibly homozygous	116821837
10	91191070	91191071	C	G	59	GENIC	possibly homozygous	116821839
10	91192382	91192383	C	T	64	GENIC	homozygous	116821841
10	91191439	91191440	G	C	48	GENIC	homozygous	116905505
10	91194089	91194090	C	T	24	GENIC	heterozygous	118049282
10	91194461	91194462	T	C	69	GENIC	possibly homozygous	118049283
10	91196422	91196423	T	G	38	GENIC	homozygous	116677054
10	91196548	91196549	A	G	78	GENIC	homozygous	116821845
10	91199030	91199031	C	T	62	GENIC	homozygous	116821851
10	91199369	91199370	T	C	79	GENIC	possibly homozygous	116821854