chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	71021787	71021788	A	C	11	GENIC	homozygous	111606086
3	71022440	71022441	A	G	26	GENIC	homozygous	111606087
3	71022479	71022480	C	G	20	GENIC	homozygous	111606088
3	71022719	71022720	A	G	11	GENIC	homozygous	111606089
3	71023093	71023094	C	T	18	GENIC	homozygous	111606090
3	71024287	71024288	C	T	14	GENIC	homozygous	111606091
3	71026787	71026788	G	A	19	GENIC	homozygous	111606092
3	71029749	71029750	G	A	23	GENIC	homozygous	111606093
3	71030674	71030675	G	A	14	GENIC	homozygous	111606095
3	71031177	71031178	T	A	21	GENIC	homozygous	111606096
3	71031253	71031254	C	A	16	GENIC	homozygous	111606097
3	71032024	71032025	T	G	5	GENIC	homozygous	111606098
3	71033515	71033516	G	A	4	GENIC	homozygous	111606099
3	71034064	71034065	G	A	19	GENIC	homozygous	111606100
3	71035318	71035319	G	T	5	GENIC	homozygous	125825847
3	71035687	71035688	T	G	20	GENIC	heterozygous	125825848
3	71036919	71036920	C	T	5	GENIC	homozygous	125825849
3	71037340	71037341	G	T	9	GENIC	homozygous	111606102
3	71038190	71038191	A	G	7	GENIC	heterozygous	125825850
3	71038449	71038450	A	G	14	GENIC	homozygous	111606103