chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	12583262	12583263	T	C	12	GENIC	heterozygous	45686003
20	12583594	12583595	G	A	12	GENIC	homozygous	45686004
20	12583600	12583601	A	C	9	GENIC	homozygous	45686005
20	12583601	12583602	T	C	9	GENIC	homozygous	45686006
20	12583918	12583919	C	T	20	GENIC	homozygous	45779523
20	12584082	12584083	C	T	29	GENIC	possibly homozygous	45779524
20	12584209	12584210	G	A	25	GENIC	homozygous	45779525
20	12584304	12584305	A	G	23	GENIC	possibly homozygous	45686008
20	12585542	12585543	C	A	23	GENIC	homozygous	45686009
20	12585686	12585687	C	T	13	GENIC	homozygous	45686010
20	12585943	12585944	C	T	21	GENIC	possibly homozygous	45779526
20	12586062	12586063	T	C	12	GENIC	homozygous	45779527
20	12586098	12586099	C	T	11	GENIC	homozygous	45779528
20	12586497	12586498	A	G	20	GENIC	possibly homozygous	45779529
20	12587747	12587748	G	A	27	GENIC	homozygous	45779530
20	12589267	12589268	T	C	25	GENIC	possibly homozygous	45686013
20	12589627	12589628	A	G	9	GENIC	homozygous	45686014
20	12589632	12589633	A	G	10	GENIC	possibly homozygous	45779531
20	12589750	12589751	G	C	9	GENIC	homozygous	45686016
20	12589779	12589780	C	T	10	GENIC	homozygous	45779532
20	12589815	12589816	T	C	17	GENIC	homozygous	45686017
20	12589965	12589966	A	-	11	GENIC	homozygous	45686018
20	12590352	12590353	A	AG	15	GENIC	possibly homozygous	45686021
20	12590584	12590585	T	G	30	GENIC	possibly homozygous	45686022
20	12590781	12590782	T	C	22	GENIC	possibly homozygous	45686024
20	12592195	12592198	GGG	---	1	GENIC	homozygous	45779534
20	12592880	12592881	A	G	22	GENIC	homozygous	45779535