chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	76360011	76360012	T	C	29	GENIC	homozygous	111095057
17	76360182	76360183	C	G	36	GENIC	homozygous	111279052
17	76362232	76362233	G	A	26	GENIC	homozygous	111213276
17	76363239	76363240	T	C	16	GENIC	homozygous	111279054
17	76364091	76364092	A	T	27	GENIC	homozygous	111279056
17	76365709	76365710	T	C	12	GENIC	homozygous	111095065
17	76366648	76366649	G	A	12	GENIC	homozygous	111279058
17	76367678	76367679	A	G	15	GENIC	homozygous	111095075
17	76367730	76367731	C	G	13	GENIC	homozygous	111279060
17	76368045	76368046	T	A	12	GENIC	homozygous	111279062
17	76368140	76368141	G	C	27	GENIC	homozygous	111279064
17	76368394	76368395	C	A	20	GENIC	homozygous	111213281
17	76369689	76369690	A	G	32	GENIC	homozygous	111279066
17	76369881	76369882	C	T	30	GENIC	homozygous	111279068
17	76370434	76370435	T	C	41	GENIC	homozygous	111213284
17	76370554	76370555	T	C	25	GENIC	homozygous	111279070
17	76370716	76370717	T	G	27	GENIC	homozygous	111095079
17	76371160	76371161	A	C	23	GENIC	homozygous	111213288
17	76371604	76371605	G	C	21	GENIC	homozygous	111279072
17	76373163	76373164	C	T	15	GENIC	homozygous	111095083
17	76373710	76373711	T	C	22	GENIC	homozygous	111095087
17	76373983	76373984	A	C	37	GENIC	homozygous	111095088
17	76375644	76375645	C	T	15	GENIC	homozygous	111279074
17	76376317	76376318	A	G	23	GENIC	homozygous	111095094
17	76377512	76377513	T	C	24	GENIC	possibly homozygous	111095098
17	76381637	76381638	A	G	13	GENIC	homozygous	111095104
17	76381645	76381646	T	C	15	GENIC	homozygous	111095106
17	76383134	76383135	T	C	18	GENIC	homozygous	111095116
17	76383139	76383140	T	C	16	GENIC	homozygous	111279076
17	76384623	76384624	G	T	39	GENIC	homozygous	111279078