chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	31858824	31858825	G	-	5	GENIC	heterozygous	50931857
12	31858826	31858827	C	CCAAGGAT	5	GENIC	heterozygous	50931860
12	31859141	31859143	GG	--	9	GENIC	heterozygous	50510224
12	31859615	31859616	A	AT	1	GENIC	homozygous	50609695
12	31859766	31859767	T	C	9	GENIC	heterozygous	50174536
12	31863377	31863378	G	A	20	GENIC	homozygous	50931863
12	31863756	31863757	C	A	18	GENIC	possibly homozygous	50931866
12	31863835	31863836	A	T	14	GENIC	possibly homozygous	50174539
12	31863865	31863866	C	G	13	GENIC	heterozygous	50672015
12	31864583	31864584	A	G	15	GENIC	possibly homozygous	50174540
12	31864659	31864660	T	G	15	GENIC	possibly homozygous	50174541
12	31865149	31865150	A	AT	8	GENIC	possibly homozygous	50931869
12	31865305	31865306	C	T	3	GENIC	homozygous	50931872
12	31865856	31865859	TTT	---	3	GENIC	heterozygous	51017577
12	31866056	31866057	T	TA	6	GENIC	heterozygous	50931875
12	31866057	31866058	T	A	6	GENIC	heterozygous	50174548
12	31866269	31866271	TT	--	1	GENIC	homozygous	50174549
12	31866580	31866581	C	T	16	GENIC	homozygous	50931878