chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40911047	40911048	G	GA	18	GENIC	heterozygous	50323516
12	40912021	40912022	C	T	26	GENIC	possibly homozygous	50323518
12	40912070	40912071	T	C	22	GENIC	homozygous	50205005
12	40913010	40913011	G	A	22	GENIC	homozygous	50323520
12	40913630	40913631	A	AAC	7	GENIC	possibly homozygous	50543799
12	40914306	40914307	T	C	30	GENIC	homozygous	50205006
12	40914573	40914574	G	T	20	GENIC	homozygous	50205007
12	40914712	40914714	TT	--	15	GENIC	heterozygous	50323524
12	40914713	40914714	T	-	15	GENIC	heterozygous	50205008
12	40915753	40915754	T	TTCTCCCAAG	26	GENIC	homozygous	50205010
12	40916039	40916040	C	-	12	GENIC	homozygous	50323526
12	40916041	40916057	TTTGAAAAGGCAAGCG	----------------	12	GENIC	homozygous	50323528
12	40917344	40917345	A	G	23	GENIC	homozygous	50205012
12	40917592	40917593	T	TG	12	GENIC	homozygous	50205013
12	40917780	40917781	T	C	12	GENIC	homozygous	50205014