chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	101161624	101161625	T	C	21	GENIC	homozygous	108165054
1	101161628	101161629	T	C	21	GENIC	homozygous	108165055
1	101161704	101161705	T	G	22	GENIC	possibly homozygous	108165056
1	101163121	101163122	T	C	64	GENIC	homozygous	108899922
1	101163780	101163781	C	T	41	GENIC	homozygous	108899924
1	101164806	101164807	C	T	24	GENIC	homozygous	108899926
1	101168673	101168674	A		33	GENIC	possibly homozygous	132530260
1	101163461	101163462	G		43	GENIC	homozygous	132530257
1	101164466	101164475	CACCACCAC		28	GENIC	homozygous	132530258
1	101164614	101164614		C	11	GENIC	homozygous	132530259
1	101164240	101164241	A		36	GENIC	homozygous	127408703
1	101169019	101169020	T	C	29	GENIC	homozygous	108899927
1	101169658	101169659	T	C	35	GENIC	homozygous	108899929
1	101171014	101171015	C	G	34	GENIC	homozygous	108899931
1	101171038	101171039	T	G	35	GENIC	homozygous	108899933
1	101171395	101171396	A	G	31	GENIC	homozygous	108899935
1	101171585	101171586	T	C	33	GENIC	homozygous	108899937