chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	31461768	31461769	T	C	13	GENIC	homozygous	51391624
10	31463347	31463348	C	-	4	GENIC	heterozygous	51391625
10	31464230	31464231	G	T	4	GENIC	heterozygous	51391626
10	31465463	31465464	T	G	15	GENIC	homozygous	51391627
10	31465773	31465774	T	G	4	GENIC	homozygous	52315963
10	31465776	31465777	T	G	11	GENIC	homozygous	51391629
10	31467453	31467454	T	C	28	GENIC	possibly homozygous	51391631
10	31468732	31468733	T	A	16	GENIC	homozygous	51391632
10	31470005	31470006	T	TG	1	GENIC	homozygous	51391633
10	31470167	31470168	A	-	9	GENIC	homozygous	51391634
10	31470181	31470182	T	-	7	GENIC	homozygous	51391635
10	31471097	31471098	T	A	10	GENIC	heterozygous	51391638
10	31471947	31471948	T	C	6	GENIC	heterozygous	51391640
10	31472812	31472813	T	C	14	GENIC	homozygous	51391641
10	31472945	31472946	T	A	22	GENIC	possibly homozygous	51391642
10	31473075	31473115	TTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC	----------------------------------------	1	GENIC	homozygous	52315964
10	31473296	31473297	C	T	22	GENIC	homozygous	51391644
10	31473340	31473341	T	G	14	GENIC	possibly homozygous	51391645
10	31473700	31473701	A	-	8	GENIC	homozygous	51391648