chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	101481639	101481640	T	C	28	GENIC	homozygous	108900520
1	101482704	101482705	G	C	32	GENIC	homozygous	108900522
1	101483500	101483501	T	C	33	GENIC	homozygous	108900526
1	101483519	101483520	G	C	36	GENIC	homozygous	108900527
1	101484992	101484993	T	C	17	GENIC	homozygous	108900535
1	101485168	101485169	T	A	9	GENIC	homozygous	108900537
1	101487223	101487224	G	A	26	GENIC	homozygous	108900539
1	101487518	101487519	A	G	25	GENIC	homozygous	108900541
1	101487791	101487792	A	G	17	GENIC	homozygous	108900543
1	101487885	101487886	A	T	16	GENIC	homozygous	108900545
1	101487977	101487978	C	T	18	GENIC	homozygous	108900547
1	101489186	101489187	T	G	35	GENIC	homozygous	108900549
1	101490005	101490006	T	A	21	GENIC	homozygous	108900550
1	101490517	101490518	A	G	42	GENIC	homozygous	108900552
1	101492070	101492071	T	C	34	GENIC	homozygous	108900554
1	101494007	101494008	A	G	29	GENIC	homozygous	108900556
1	101494084	101494085	G	T	17	GENIC	homozygous	108900557
1	101494989	101494990	T	G	24	GENIC	homozygous	108900559
1	101495417	101495418	G	T	22	GENIC	homozygous	108900561
1	101495719	101495720	C	T	31	GENIC	homozygous	108900563
1	101497418	101497419	C	T	36	GENIC	homozygous	108900564
1	101502324	101502325	A	C	20	GENIC	homozygous	108900571
1	101502870	101502871	G	A	15	GENIC	homozygous	108900575
1	101504015	101504016	T	C	27	GENIC	homozygous	108900577
1	101505065	101505066	G	A	29	GENIC	homozygous	108900579
1	101505334	101505335	C	T	17	GENIC	homozygous	108900581
1	101506936	101506937	C	A	23	GENIC	homozygous	108900583
1	101507221	101507222	G	A	21	GENIC	homozygous	108900585
1	101507255	101507256	G	A	24	GENIC	homozygous	108900587
1	101508166	101508167	C	A	30	GENIC	homozygous	108900589