chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	43081676	43081677	G	A	12	GENIC	homozygous	46256627
19	43086916	43086917	T	TG	19	GENIC	possibly homozygous	46256628
19	43087456	43087457	G	A	21	GENIC	homozygous	46256629
19	43095356	43095357	T	TG	13	GENIC	homozygous	46138280
19	43097092	43097093	C	CTG	6	GENIC	heterozygous	46138290
19	43097092	43097093	C	CTGTGTGTGTG	6	GENIC	heterozygous	46405742
19	43092468	43092469	C	CT	13	GENIC	heterozygous	46462095
19	43103898	43103899	A	T	18	GENIC	homozygous	46138311
19	43104966	43104967	G	A	10	GENIC	homozygous	46256630
19	43106619	43106620	G	GGTGTGTGTGTGT	5	GENIC	heterozygous	46405746
19	43110286	43110287	A	-	4	GENIC	heterozygous	46462097
19	43116257	43116300	TTTTTGTCGAGTGTGCCGGTACACACGTATGTTATACCTATGA	-------------------------------------------	15	GENIC	homozygous	46405750
19	43124493	43124494	T	TTC	1	GENIC	homozygous	46656036
19	43124896	43124897	T	C	15	GENIC	homozygous	46138399
19	43125080	43125081	G	T	22	GENIC	homozygous	46256632
19	43127808	43127809	C	CGCCCTGA	21	GENIC	homozygous	46256633
19	43130460	43130461	G	GA	12	GENIC	heterozygous	46380461
19	43131076	43131077	C	CA	11	GENIC	heterozygous	46552640
19	43141077	43141078	G	A	24	GENIC	homozygous	46256635
19	43143073	43143074	G	A	17	GENIC	homozygous	46138426
19	43143616	43143620	TGTT	----	10	GENIC	homozygous	46256636
19	43145123	43145124	G	GT	9	GENIC	heterozygous	46256637
19	43106620	43106622	GT	--	5	GENIC	heterozygous	46669995