chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	31402751	31402752	C	T	17	GENIC	homozygous	111026011
17	31403287	31403288	T	C	21	GENIC	homozygous	111026013
17	31403387	31403388	T	C	24	GENIC	homozygous	111026015
17	31404628	31404629	C	T	36	GENIC	homozygous	111189850
17	31406587	31406588	C	T	15	GENIC	homozygous	111026019
17	31406652	31406653	G	A	10	GENIC	homozygous	111026021
17	31407045	31407046	C	T	20	GENIC	possibly homozygous	111026023
17	31407244	31407245	G	A	17	GENIC	homozygous	111026025
17	31407413	31407414	G	A	27	GENIC	homozygous	111026027
17	31407431	31407432	A	G	28	GENIC	homozygous	111026029
17	31407840	31407841	T	C	17	GENIC	homozygous	111026031
17	31408327	31408328	G	A	14	GENIC	homozygous	111026033
17	31408510	31408511	G	A	16	GENIC	homozygous	111026035
17	31408724	31408725	G	A	15	GENIC	homozygous	111026037
17	31408992	31408993	A	G	13	GENIC	homozygous	111026039
17	31409016	31409017	T	A	18	GENIC	homozygous	111026041
17	31410064	31410065	G	A	14	GENIC	homozygous	111026042
17	31410209	31410210	A	G	20	GENIC	homozygous	111026044
17	31410834	31410835	C	T	21	GENIC	homozygous	111026046
17	31411031	31411032	A	C	14	GENIC	homozygous	111026048
17	31411434	31411435	G	T	8	GENIC	homozygous	111026050
17	31411535	31411536	T	C	5	GENIC	homozygous	111026052