chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	104006002	104006003	A	C	20	GENIC	homozygous	109958073
2	104006542	104006543	G	A	10	GENIC	homozygous	109958075
2	104006580	104006581	T	C	8	GENIC	homozygous	109958077
2	104007893	104007894	T	C	40	GENIC	heterozygous	110578641
2	104009018	104009019	T	C	27	GENIC	homozygous	109958079
2	104010420	104010421	A	C	24	GENIC	possibly homozygous	109958081
2	104011879	104011880	C	T	26	GENIC	homozygous	109958083
2	104011924	104011925	T	C	33	GENIC	homozygous	109958084
2	104016403	104016404	T	C	23	GENIC	homozygous	109958088
2	104016907	104016908	C	T	25	GENIC	homozygous	109958090
2	104018154	104018155	C	T	23	GENIC	possibly homozygous	109958092
2	104020195	104020196	T	A	28	GENIC	homozygous	109958094
2	104024435	104024436	A	G	22	GENIC	homozygous	109958096
2	104024582	104024583	G	A	10	GENIC	heterozygous	109958098
2	104024584	104024585	G	A	11	GENIC	heterozygous	109958100
2	104025110	104025111	T	A	27	GENIC	homozygous	109958102
2	104026060	104026061	C	T	26	GENIC	homozygous	109958104
2	104026954	104026955	A	G	27	GENIC	homozygous	109958106
2	104028808	104028809	C	T	13	GENIC	homozygous	110578645
2	104029629	104029630	G	A	19	GENIC	homozygous	109958108
2	104032019	104032020	T	C	23	GENIC	homozygous	109958109
2	104032325	104032326	G	C	33	GENIC	homozygous	109958111
2	104034300	104034301	C	G	36	GENIC	homozygous	109958113
2	104034534	104034535	G	A	29	GENIC	homozygous	109958115
2	104036112	104036113	T	G	27	GENIC	homozygous	109958117
2	104038469	104038470	G	A	25	GENIC	homozygous	109958119
2	104038522	104038523	T	C	31	GENIC	homozygous	109958120
2	104039643	104039644	C	T	33	GENIC	homozygous	109958124
2	104040500	104040501	C	G	19	GENIC	homozygous	109958126
2	104040544	104040545	A	G	23	GENIC	homozygous	109958128