chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	85150416	85150417	G	A	11	GENIC	heterozygous	132697168
10	85150418	85150419	T	A	11	GENIC	heterozygous	132697169
10	85150423	85150424	T	A	13	GENIC	heterozygous	132697170
10	85150426	85150427	T	A	13	GENIC	heterozygous	132697171
10	85156188	85156189	G	T	14	GENIC	homozygous	117226971
10	85173627	85173628	C	A	11	GENIC	heterozygous	118004796
10	85203358	85203359	A	C	41	GENIC	heterozygous	132697172
10	85203368	85203369	G	A	41	GENIC	heterozygous	132697173
10	85203386	85203387	T	A	39	GENIC	heterozygous	132697174
10	85203392	85203393	T	C	38	GENIC	heterozygous	132697175
10	85203393	85203394	T	C	38	GENIC	heterozygous	132697176
10	85203395	85203396	G	A	38	GENIC	heterozygous	132697177
10	85204101	85204102	A		23	GENIC	heterozygous	132331561
10	85204386	85204387	A		30	GENIC	heterozygous	130394035
10	85215661	85215662	T	C	28	GENIC	homozygous	116665331
10	85216066	85216067	T		21	GENIC	heterozygous	130394036
10	85216777	85216778	T	G	11	GENIC	homozygous	116665333
10	85165118	85165119	T	A	33	GENIC	possibly homozygous	116948422
10	85203409	85203409		TGTGTCTGAAGA	36	GENIC	heterozygous	132693637