chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	42133510	42133511	A	C	19	GENIC	homozygous	111049578
17	42134123	42134124	G	A	20	GENIC	homozygous	111049580
17	42134575	42134576	A	G	20	GENIC	homozygous	111049582
17	42135510	42135511	A	C	10	GENIC	homozygous	111049584
17	42135820	42135821	C	T	19	GENIC	homozygous	111203479
17	42135925	42135926	G	A	16	GENIC	homozygous	111203480
17	42136336	42136337	T	C	26	GENIC	homozygous	111203481
17	42137037	42137038	G	A	19	GENIC	homozygous	111049589
17	42137207	42137208	A	G	18	GENIC	homozygous	111306360
17	42137982	42137983	T	C	20	GENIC	homozygous	111049591
17	42138556	42138557	A	G	11	GENIC	homozygous	111049593
17	42139869	42139870	A	G	13	GENIC	homozygous	111049597
17	42141516	42141517	G	T	6	GENIC	homozygous	111049599
17	42141940	42141941	T	C	9	GENIC	homozygous	111203482
17	42143198	42143199	C	T	13	GENIC	homozygous	111049601
17	42143613	42143614	T	C	12	GENIC	homozygous	111049603
17	42145319	42145320	G	A	28	GENIC	homozygous	111203483
17	42145738	42145739	A	G	15	GENIC	homozygous	111049605
17	42145986	42145987	G	A	19	GENIC	homozygous	111049607
17	42149435	42149436	T	C	15	GENIC	homozygous	111049611
17	42152169	42152170	T	C	16	GENIC	homozygous	111049615
17	42153593	42153594	C	T	32	GENIC	homozygous	111203484
17	42155488	42155489	C	G	20	GENIC	homozygous	111049617
17	42155721	42155722	G	A	18	GENIC	homozygous	111203485
17	42156741	42156742	C	T	26	GENIC	homozygous	111203486
17	42157513	42157514	A	G	28	GENIC	homozygous	111049621