chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	51847937	51847938	C	-	9	INTERGENIC	homozygous	51102161
12	51847948	51847949	C	A	8	INTERGENIC	homozygous	50514147
12	51850086	51850087	G	C	8	GENIC	homozygous	50247949
12	51850408	51850409	C	A	10	GENIC	homozygous	50247951
12	51850563	51850564	A	G	9	GENIC	homozygous	50247953
12	51850632	51850633	C	T	9	GENIC	homozygous	50247955
12	51850645	51850646	A	G	8	GENIC	homozygous	50247957
12	51850996	51850997	T	C	12	GENIC	homozygous	50247959
12	51852985	51852989	CCCT	----	17	GENIC	homozygous	50247965
12	51853953	51853954	A	G	13	GENIC	homozygous	50247967
12	51870460	51870468	CTAGGTTA	--------	10	GENIC	homozygous	50247969
12	51870854	51870855	A	G	14	GENIC	homozygous	50247971
12	51871389	51871390	C	T	9	GENIC	homozygous	50247973
12	51871599	51871600	T	C	21	GENIC	homozygous	50247975
12	51872306	51872307	T	-	20	GENIC	homozygous	50247983
12	51872307	51872308	G	A	20	GENIC	homozygous	51102163
12	51872492	51872493	G	T	12	GENIC	homozygous	50247985
12	51872836	51872837	A	G	16	GENIC	homozygous	50247987
12	51873249	51873250	A	G	17	GENIC	homozygous	50247991
12	51873586	51873587	T	C	16	GENIC	homozygous	50247993
12	51873985	51873986	C	CAG	8	GENIC	homozygous	50248004
12	51874099	51874100	T	C	11	GENIC	homozygous	50248006
12	51874158	51874159	G	A	8	GENIC	homozygous	50248008
12	51875195	51875196	G	A	8	GENIC	homozygous	50248012
12	51875201	51875202	G	A	7	GENIC	homozygous	50248014
12	51875714	51875715	G	A	11	GENIC	homozygous	50248018
12	51875994	51875995	A	G	17	GENIC	homozygous	50248020
12	51877005	51877006	T	TC	9	GENIC	homozygous	50248045
12	51877948	51877949	T	C	15	GENIC	homozygous	50248047