chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91186938	91186939	A	G	11	GENIC	homozygous	116821825
10	91187653	91187654	A	G	4	GENIC	homozygous	116821831
10	91187792	91187793	A	G	4	GENIC	homozygous	116821833
10	91189741	91189742	A	C	19	GENIC	homozygous	116821835
10	91190880	91190881	G	T	10	GENIC	homozygous	116905503
10	91191439	91191440	G	C	12	GENIC	homozygous	116905505
10	91193213	91193214	T	C	16	GENIC	homozygous	116905507
10	91193632	91193633	C	T	13	GENIC	homozygous	116951792
10	91193986	91193987	T	A	10	GENIC	homozygous	116905509
10	91194572	91194573	T	C	6	GENIC	homozygous	116905511
10	91194843	91194844	T	G	15	GENIC	heterozygous	116905519
10	91194898	91194899	T	C	5	GENIC	homozygous	117392123
10	91195423	91195424	T	C	3	GENIC	heterozygous	116951794
10	91196422	91196423	T	G	21	GENIC	homozygous	116677054
10	91196548	91196549	A	G	14	GENIC	homozygous	116821845
10	91196592	91196593	T	A	8	GENIC	homozygous	116905521
10	91196715	91196716	T	C	8	GENIC	homozygous	116905523
10	91197610	91197611	A	G	20	GENIC	homozygous	116905525
10	91199426	91199427	A	G	17	GENIC	homozygous	116905529