chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	48456610	48456611	T	G	35	GENIC	homozygous	114669494
13	48458865	48458866	T	G	28	GENIC	heterozygous	114337884
13	48458875	48458876	T	C	25	GENIC	homozygous	114337888
13	48458886	48458887	T	C	25	GENIC	homozygous	114337890
13	48458889	48458890	C	A	25	GENIC	homozygous	114337892
13	48458981	48458982	T	A	42	GENIC	homozygous	114669496
13	48459706	48459707	C	T	16	GENIC	homozygous	114669498
13	48459811	48459812	T	C	27	GENIC	possibly homozygous	114549207
13	48460507	48460508	A	C	9	GENIC	homozygous	114549208
13	48460671	48460672	G	C	30	GENIC	homozygous	114549209
13	48460891	48460892	G	A	32	GENIC	homozygous	114549210
13	48461170	48461171	C	T	22	GENIC	homozygous	114669500
13	48462212	48462213	A	G	21	GENIC	homozygous	114549212
13	48462609	48462610	G	A	17	GENIC	homozygous	114669502
13	48463673	48463674	G	A	24	GENIC	homozygous	114669504
13	48465549	48465550	A	G	26	GENIC	homozygous	114549215
13	48466189	48466190	T	G	38	GENIC	homozygous	114669506
13	48468747	48468748	T	C	31	GENIC	homozygous	114549218
13	48468912	48468913	T	C	27	GENIC	homozygous	114549219
13	48469459	48469460	G	C	16	GENIC	homozygous	114549220
13	48469875	48469876	A	G	24	GENIC	homozygous	114549221
13	48470893	48470894	A	G	40	GENIC	heterozygous	118497825
13	48470902	48470903	G	T	45	GENIC	heterozygous	114857465
13	48470736	48470737	G	A	22	GENIC	homozygous	114720066
13	48470896	48470897	T	G	42	GENIC	heterozygous	118535361
13	48472057	48472058	T	C	15	GENIC	homozygous	114669508
13	48472204	48472205	A	G	27	GENIC	homozygous	114549222
13	48472483	48472484	T	C	32	GENIC	homozygous	114720068
13	48473522	48473523	A	G	28	GENIC	homozygous	114549223
13	48474096	48474097	A	G	29	GENIC	homozygous	114549224
13	48475554	48475555	T	G	27	GENIC	homozygous	114669510
13	48475671	48475672	C	T	21	GENIC	homozygous	114669512
13	48475898	48475899	G	A	24	GENIC	homozygous	114669514
13	48475928	48475929	A	G	25	GENIC	homozygous	114549225
13	48476743	48476744	T	C	35	GENIC	homozygous	114549228