chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	31461768	31461769	T	C	21	GENIC	homozygous	51391624
10	31463347	31463348	C	-	13	GENIC	homozygous	51391625
10	31463497	31463512	AACAACAACAAAAAA	---------------	4	GENIC	homozygous	52365297
10	31464230	31464231	G	T	7	GENIC	homozygous	51391626
10	31465463	31465464	T	G	22	GENIC	homozygous	51391627
10	31465776	31465777	T	G	26	GENIC	homozygous	51391629
10	31466464	31466465	A	AAGAGAGAG	5	GENIC	homozygous	51391630
10	31467453	31467454	T	C	31	GENIC	homozygous	51391631
10	31468732	31468733	T	A	18	GENIC	homozygous	51391632
10	31470005	31470006	T	TG	3	GENIC	heterozygous	51391633
10	31470167	31470168	A	-	15	GENIC	homozygous	51391634
10	31470181	31470182	T	-	14	GENIC	homozygous	51391635
10	31470418	31470419	T	TCCC	20	GENIC	homozygous	51391636
10	31471097	31471098	T	A	13	GENIC	homozygous	51391638
10	31471770	31471771	C	CT	3	GENIC	homozygous	51391639
10	31471947	31471948	T	C	17	GENIC	homozygous	51391640
10	31472812	31472813	T	C	16	GENIC	homozygous	51391641
10	31472945	31472946	T	A	23	GENIC	homozygous	51391642
10	31473296	31473297	C	T	35	GENIC	homozygous	51391644
10	31473340	31473341	T	G	30	GENIC	homozygous	51391645
10	31473628	31473632	CACA	----	7	GENIC	homozygous	52365299
10	31473700	31473701	A	-	19	GENIC	homozygous	51391648
10	31474297	31474298	T	TTTTC	6	GENIC	heterozygous	51391649
10	31474562	31474563	C	CGTGTGT	17	GENIC	heterozygous	51391650
10	31474562	31474563	C	CGTGTGTGT	17	GENIC	possibly homozygous	51391651
10	31465773	31465774	T	G	20	GENIC	homozygous	52315963
10	31473075	31473115	TTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC	----------------------------------------	18	GENIC	homozygous	52315964
10	31474193	31474194	A	-	12	GENIC	homozygous	52185633