chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	43473470	43473471	C	T	39	GENIC	homozygous	111053152
17	43473617	43473618	G	A	41	GENIC	homozygous	111053154
17	43473858	43473859	C	T	26	GENIC	homozygous	111053156
17	43474889	43474890	G	C	33	GENIC	homozygous	111053160
17	43475678	43475679	G	A	27	GENIC	homozygous	111053162
17	43476436	43476437	T	C	38	GENIC	homozygous	111053164
17	43476918	43476919	T	C	29	GENIC	homozygous	111053166
17	43477293	43477294	G	C	27	GENIC	homozygous	111053168
17	43477452	43477453	G	T	26	GENIC	homozygous	111053170
17	43479123	43479124	C	T	21	GENIC	homozygous	111053172
17	43479298	43479299	G	A	33	GENIC	homozygous	111053174
17	43479968	43479969	T	A	40	GENIC	homozygous	111053176
17	43481525	43481526	C	A	28	GENIC	homozygous	111053178
17	43482535	43482536	T	C	36	GENIC	homozygous	111053180
17	43484390	43484391	C	G	19	GENIC	homozygous	111053182
17	43482004	43482005	C	T	28	GENIC	possibly homozygous	111244667
17	43489046	43489047	A	G	28	GENIC	homozygous	111053186
17	43489315	43489316	C	A	27	GENIC	homozygous	111390004
17	43489575	43489576	G	T	5	GENIC	homozygous	111053188
17	43490998	43490999	T	C	27	GENIC	homozygous	111053192
17	43491143	43491144	G	T	34	GENIC	homozygous	111053194
17	43491892	43491893	G	T	32	GENIC	homozygous	111244669
17	43493277	43493278	G	A	26	GENIC	homozygous	111053196
17	43493579	43493580	C	T	29	GENIC	homozygous	111053198
17	43495561	43495562	G	C	43	GENIC	homozygous	111053200
17	43495805	43495806	C	T	33	GENIC	homozygous	111053202
17	43496905	43496906	T	C	26	GENIC	homozygous	111053204
17	43497448	43497449	T	G	21	GENIC	homozygous	111053206