chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	42133510	42133511	A	C	14	GENIC	homozygous	111049578
17	42134123	42134124	G	A	19	GENIC	homozygous	111049580
17	42134575	42134576	A	G	27	GENIC	homozygous	111049582
17	42135510	42135511	A	C	16	GENIC	homozygous	111049584
17	42135820	42135821	C	T	24	GENIC	homozygous	111203479
17	42136336	42136337	T	C	19	GENIC	homozygous	111203481
17	42137037	42137038	G	A	22	GENIC	homozygous	111049589
17	42137982	42137983	T	C	26	GENIC	homozygous	111049591
17	42138556	42138557	A	G	21	GENIC	homozygous	111049593
17	42139869	42139870	A	G	25	GENIC	homozygous	111049597
17	42141516	42141517	G	T	17	GENIC	homozygous	111049599
17	42143198	42143199	C	T	28	GENIC	homozygous	111049601
17	42143613	42143614	T	C	27	GENIC	homozygous	111049603
17	42145738	42145739	A	G	29	GENIC	homozygous	111049605
17	42145986	42145987	G	A	27	GENIC	homozygous	111049607
17	42149435	42149436	T	C	33	GENIC	homozygous	111049611
17	42152169	42152170	T	C	17	GENIC	homozygous	111049615
17	42155488	42155489	C	G	25	GENIC	homozygous	111049617
17	42157513	42157514	A	G	19	GENIC	homozygous	111049621
17	42137207	42137208	A	G	16	GENIC	homozygous	111306360
17	42153548	42153549	G	A	22	GENIC	homozygous	111306361
17	42155473	42155474	T	G	25	GENIC	homozygous	111306362