chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10586126	10586127	C	A	5	GENIC	homozygous	110954433
17	10587410	10587411	T	G	24	GENIC	homozygous	110954437
17	10587520	10587521	T	G	23	GENIC	homozygous	111524992
17	10587799	10587800	G	T	17	GENIC	homozygous	111231022
17	10587978	10587979	A	G	25	GENIC	homozygous	111524994
17	10588318	10588319	C	T	16	GENIC	homozygous	111524996
17	10588387	10588388	C	T	15	GENIC	homozygous	111524998
17	10588918	10588919	C	A	26	GENIC	homozygous	111525000
17	10588953	10588954	A	G	27	GENIC	homozygous	110954439
17	10589160	10589161	C	T	23	GENIC	homozygous	111525002
17	10589775	10589776	T	C	11	GENIC	homozygous	111525004
17	10590243	10590244	T	G	14	GENIC	homozygous	111525006
17	10591823	10591824	T	C	18	GENIC	homozygous	111525008
17	10591961	10591962	C	G	12	GENIC	homozygous	111525010
17	10592139	10592140	T	A	16	GENIC	homozygous	111525012
17	10592547	10592548	A	G	15	GENIC	homozygous	111525014
17	10592637	10592638	G	A	16	GENIC	homozygous	111525016
17	10592976	10592977	A	C	16	GENIC	homozygous	111525018
17	10593112	10593113	A	G	23	GENIC	homozygous	110954443
17	10593401	10593402	C	T	20	GENIC	homozygous	110954449
17	10593779	10593780	C	A	25	GENIC	homozygous	110954453
17	10593879	10593880	G	A	16	GENIC	homozygous	111525020
17	10594930	10594931	C	T	32	GENIC	homozygous	110954461
17	10595164	10595165	A	G	14	GENIC	homozygous	110954463
17	10595412	10595413	A	G	25	GENIC	homozygous	110954467
17	10597220	10597221	G	A	15	GENIC	homozygous	111525022