chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40911047	40911048	G	GA	14	GENIC	possibly homozygous	50323516
12	40912021	40912022	C	T	53	GENIC	homozygous	50323518
12	40912070	40912071	T	C	56	GENIC	homozygous	50205005
12	40913010	40913011	G	A	63	GENIC	homozygous	50323520
12	40914306	40914307	T	C	40	GENIC	homozygous	50205006
12	40914573	40914574	G	T	39	GENIC	possibly homozygous	50205007
12	40914712	40914714	TT	--	6	GENIC	heterozygous	50323524
12	40914713	40914714	T	-	6	GENIC	heterozygous	50205008
12	40915753	40915754	T	TTCTCCCAAG	21	GENIC	homozygous	50205010
12	40916039	40916040	C	-	12	GENIC	homozygous	50323526
12	40916041	40916057	TTTGAAAAGGCAAGCG	----------------	11	GENIC	homozygous	50323528
12	40916203	40916204	C	-	8	GENIC	heterozygous	50323530
12	40917344	40917345	A	G	47	GENIC	homozygous	50205012
12	40917592	40917593	T	TG	10	GENIC	homozygous	50205013
12	40917780	40917781	T	C	20	GENIC	homozygous	50205014
12	40915059	40915060	A	G	53	GENIC	heterozygous	50486376