chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	9778394	9778395	T	G	16	GENIC	homozygous	110953097
17	9780889	9780890	A	G	18	GENIC	homozygous	110953099
17	9781021	9781022	C	G	11	GENIC	homozygous	110953101
17	9781199	9781200	C	G	16	GENIC	homozygous	110953103
17	9781556	9781557	T	C	13	GENIC	homozygous	110953105
17	9781614	9781615	T	C	16	GENIC	homozygous	110953107
17	9782136	9782137	A	G	26	GENIC	homozygous	110953109
17	9782246	9782247	T	C	28	GENIC	homozygous	110953111
17	9782280	9782281	G	A	25	GENIC	homozygous	110953113
17	9782343	9782344	C	T	24	GENIC	homozygous	110953115
17	9782848	9782849	A	G	21	GENIC	homozygous	110953117
17	9786612	9786613	T	C	21	GENIC	homozygous	110953119
17	9786651	9786652	T	G	11	GENIC	heterozygous	110953121
17	9787369	9787370	A	G	28	GENIC	homozygous	110953123
17	9787545	9787546	T	A	15	GENIC	homozygous	110953125
17	9788832	9788833	A	T	16	GENIC	homozygous	111332216
17	9789346	9789347	G	C	14	GENIC	homozygous	110953127
17	9789456	9789457	C	T	19	GENIC	homozygous	110953129
17	9789506	9789507	C	A	12	GENIC	homozygous	110953131
17	9789521	9789522	T	C	17	GENIC	homozygous	110953133
17	9789880	9789881	G	A	24	GENIC	homozygous	110953135
17	9790043	9790044	G	A	17	GENIC	homozygous	110953137
17	9790241	9790242	C	G	17	GENIC	homozygous	110953139
17	9790284	9790285	G	A	25	GENIC	homozygous	110953141
17	9790790	9790791	G	A	16	GENIC	homozygous	110953143
17	9791391	9791392	C	T	20	GENIC	homozygous	110953145
17	9791928	9791929	G	A	26	GENIC	homozygous	110953147