chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	12582634	12582635	T	G	14	GENIC	homozygous	45431390
20	12582637	12582638	T	G	14	GENIC	homozygous	45431391
20	12583262	12583263	T	C	14	GENIC	homozygous	45686003
20	12583594	12583595	G	A	27	GENIC	homozygous	45686004
20	12583600	12583601	A	C	27	GENIC	homozygous	45686005
20	12583601	12583602	T	C	26	GENIC	homozygous	45686006
20	12584095	12584096	C	T	28	GENIC	homozygous	45686007
20	12584304	12584305	A	G	31	GENIC	homozygous	45686008
20	12585542	12585543	C	A	34	GENIC	homozygous	45686009
20	12585686	12585687	C	T	23	GENIC	homozygous	45686010
20	12588882	12588883	T	C	20	GENIC	homozygous	45686011
20	12588915	12588916	C	G	27	GENIC	homozygous	45686012
20	12589267	12589268	T	C	28	GENIC	homozygous	45686013
20	12589627	12589628	A	G	20	GENIC	homozygous	45686014
20	12589673	12589674	C	T	20	GENIC	homozygous	45686015
20	12589750	12589751	G	C	24	GENIC	homozygous	45686016
20	12589815	12589816	T	C	19	GENIC	homozygous	45686017
20	12589965	12589966	A	-	26	GENIC	homozygous	45686018
20	12590127	12590128	T	C	31	GENIC	homozygous	45686019
20	12590148	12590149	C	T	30	GENIC	homozygous	45686020
20	12590352	12590353	A	AG	12	GENIC	homozygous	45686021
20	12590584	12590585	T	G	35	GENIC	homozygous	45686022
20	12590637	12590638	T	C	32	GENIC	homozygous	45686023
20	12590781	12590782	T	C	31	GENIC	homozygous	45686024
20	12590786	12590787	A	G	31	GENIC	homozygous	45686025
20	12591096	12591097	A	T	38	GENIC	homozygous	45686026
20	12591225	12591226	A	G	32	GENIC	homozygous	45686027
20	12591342	12591343	C	T	23	GENIC	homozygous	45686028
20	12591842	12591843	A	G	19	GENIC	homozygous	45686029
20	12592196	12592198	GG	--	9	GENIC	heterozygous	45856117
20	12592197	12592198	G	-	9	GENIC	heterozygous	45431392
20	12592431	12592432	C	T	29	GENIC	homozygous	45686030