chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	99762197	99762198	C	G	26	GENIC	homozygous	112616605
15	99762208	99762209	A	G	24	GENIC	homozygous	112616606
15	99762838	99762839	T	A	19	GENIC	homozygous	112616607
15	99762994	99762995	C	T	21	GENIC	homozygous	112616608
15	99763005	99763006	G	A	23	GENIC	homozygous	112616609
15	99763450	99763451	A	G	12	GENIC	homozygous	112616610
15	99763640	99763641	A	G	22	GENIC	homozygous	112616611
15	99763923	99763924	G	A	27	GENIC	homozygous	112616612
15	99764001	99764002	A	G	23	GENIC	homozygous	112616614
15	99764197	99764198	C	G	28	GENIC	homozygous	112616616
15	99764261	99764262	G	A	22	GENIC	homozygous	112616618
15	99764535	99764536	T	C	20	GENIC	homozygous	112616620
15	99764584	99764585	C	G	26	GENIC	homozygous	112616622
15	99764585	99764586	T	A	26	GENIC	homozygous	112616624
15	99765048	99765049	G	A	15	GENIC	homozygous	112616635
15	99765365	99765366	T	C	21	GENIC	homozygous	112616637
15	99765442	99765443	T	A	15	GENIC	homozygous	112616639
15	99765787	99765788	G	A	19	GENIC	homozygous	112616641
15	99765905	99765906	G	T	21	GENIC	homozygous	112616643
15	99766733	99766734	G	C	18	GENIC	homozygous	112616645
15	99767101	99767102	T	C	23	GENIC	homozygous	112616647
15	99767199	99767200	C	T	19	GENIC	homozygous	112616649
15	99767963	99767964	C	A	26	GENIC	homozygous	112826739
15	99768019	99768020	T	A	17	GENIC	homozygous	112760505
15	99768918	99768919	A	G	26	GENIC	homozygous	112826743
15	99770785	99770786	T	C	13	GENIC	homozygous	112616655
15	99770875	99770876	G	T	15	GENIC	homozygous	112616657
15	99770948	99770949	A	G	28	GENIC	homozygous	112616659
15	99771323	99771324	A	G	21	GENIC	homozygous	112616661
15	99771352	99771353	C	A	23	GENIC	homozygous	112616663