chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	40221417	40221418	T	C	16	GENIC	homozygous	111500042
17	40222064	40222065	T	C	19	GENIC	homozygous	111201890
17	40222858	40222859	C	T	11	GENIC	homozygous	111500044
17	40223486	40223487	C	T	15	GENIC	homozygous	111044486
17	40223659	40223660	C	T	23	GENIC	possibly homozygous	111500046
17	40223796	40223797	T	C	10	GENIC	homozygous	111500048
17	40224537	40224538	T	C	16	GENIC	homozygous	111201896
17	40224829	40224830	C	T	15	GENIC	homozygous	111500050
17	40224938	40224939	T	A	15	GENIC	homozygous	111500052
17	40225361	40225362	C	G	10	GENIC	homozygous	111201899
17	40226181	40226182	G	A	6	GENIC	homozygous	111044494
17	40226848	40226849	T	A	7	GENIC	homozygous	111044498
17	40227542	40227543	A	C	21	GENIC	possibly homozygous	119424209
17	40227672	40227673	G	T	21	GENIC	homozygous	111201900
17	40227694	40227695	G	T	26	GENIC	homozygous	111201901
17	40227905	40227906	G	T	26	GENIC	homozygous	119424211
17	40227944	40227945	T	G	17	GENIC	possibly homozygous	111500054
17	40228425	40228426	C	G	17	GENIC	homozygous	119424213
17	40228690	40228691	C	T	12	GENIC	homozygous	119424215
17	40229521	40229522	T	C	19	GENIC	homozygous	111500056
17	40229538	40229539	A	T	18	GENIC	homozygous	111201903
17	40229996	40229997	A	C	24	GENIC	homozygous	119424217
17	40230639	40230640	G	A	15	GENIC	homozygous	111044502
17	40230782	40230783	C	A	22	GENIC	possibly homozygous	111500058
17	40230924	40230925	G	T	34	GENIC	homozygous	111044504
17	40231125	40231126	A	G	19	GENIC	homozygous	111201908
17	40231208	40231209	G	T	13	GENIC	homozygous	111500060
17	40231466	40231467	A	G	8	GENIC	homozygous	111044508
17	40231614	40231615	G	A	8	GENIC	homozygous	111201910
17	40231622	40231623	T	C	9	GENIC	homozygous	111044510
17	40231666	40231667	A	G	12	GENIC	homozygous	111201911
17	40231748	40231749	T	C	11	GENIC	homozygous	111500062