chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	50792025	50792026	C	T	19	GENIC	homozygous	47127873
17	50792068	50792069	G	C	20	GENIC	homozygous	47127874
17	50792205	50792206	C	G	23	GENIC	homozygous	47127875
17	50792602	50792603	G	A	24	GENIC	homozygous	47127876
17	50792810	50792811	A	G	23	GENIC	homozygous	47127877
17	50792895	50792896	A	G	14	GENIC	homozygous	47127878
17	50793102	50793103	T	TA	17	GENIC	possibly homozygous	47127879
17	50793151	50793152	A	C	31	GENIC	homozygous	47127880
17	50793184	50793185	A	G	33	GENIC	homozygous	47127881
17	50793263	50793264	T	-	25	GENIC	homozygous	47127882
17	50793314	50793315	T	C	16	GENIC	homozygous	47127883
17	50793328	50793329	C	T	21	GENIC	homozygous	47127884
17	50793378	50793379	C	T	24	GENIC	homozygous	47127885
17	50793414	50793415	A	G	25	GENIC	homozygous	47127886
17	50793695	50793696	C	T	17	GENIC	homozygous	47127887
17	50793696	50793697	G	A	18	GENIC	homozygous	47127888
17	50793936	50793937	A	C	26	GENIC	homozygous	47127889
17	50794521	50794522	G	C	19	GENIC	homozygous	47127890
17	50794528	50794529	G	A	16	GENIC	homozygous	47127891
17	50794537	50794538	C	T	13	GENIC	homozygous	47127892
17	50794556	50794557	G	A	14	GENIC	homozygous	47127893
17	50794678	50794679	T	A	16	GENIC	homozygous	47127897
17	50795058	50795059	G	A	19	GENIC	homozygous	47127900
17	50795200	50795201	T	C	16	GENIC	homozygous	47127901
17	50795676	50795677	C	T	28	GENIC	homozygous	47127902
17	50796727	50796728	G	A	23	GENIC	homozygous	47127903
17	50796785	50796786	C	T	15	GENIC	homozygous	47127904
17	50797135	50797136	T	C	19	GENIC	homozygous	47127905
17	50797595	50797596	C	T	25	GENIC	homozygous	47127906
17	50798421	50798422	T	TGC	6	GENIC	heterozygous	47127907
17	50798521	50798522	C	T	15	GENIC	homozygous	47127911
17	50794682	50794683	A	AT	19	GENIC	homozygous	48076498
17	50795790	50795791	A	T	17	GENIC	homozygous	48076499
17	50799487	50799488	A	C	28	GENIC	homozygous	48076500