chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	50857351	50857352	T	C	10	GENIC	homozygous	46448554
18	50857958	50857961	ACA	---	3	GENIC	homozygous	46448555
18	50857963	50857964	T	-	2	GENIC	homozygous	46448556
18	50858354	50858355	G	A	12	GENIC	homozygous	46448557
18	50858454	50858455	T	TCC	2	GENIC	homozygous	46448558
18	50859212	50859213	C	T	6	GENIC	homozygous	46769691
18	50859219	50859220	G	A	2	GENIC	homozygous	46448560
18	50859348	50859349	C	T	15	GENIC	possibly homozygous	46448561
18	50859429	50859430	C	T	15	GENIC	homozygous	46769692
18	50859537	50859538	T	G	21	GENIC	possibly homozygous	46448562
18	50859731	50859732	T	C	23	GENIC	possibly homozygous	46448564
18	50859943	50859944	C	A	35	GENIC	possibly homozygous	46769693
18	50860385	50860386	A	G	18	GENIC	possibly homozygous	46448565
18	50861176	50861177	G	A	10	GENIC	heterozygous	46448568
18	50861349	50861350	C	T	8	GENIC	homozygous	46448569
18	50861660	50861661	G	A	19	GENIC	possibly homozygous	46448570
18	50862362	50862363	G	T	12	GENIC	homozygous	46448571
18	50862992	50862993	A	G	5	GENIC	homozygous	46448574
18	50863427	50863428	G	T	16	GENIC	homozygous	46448576
18	50863684	50863685	C	A	6	GENIC	homozygous	46769694
18	50863791	50863792	G	A	10	GENIC	possibly homozygous	46769695
18	50863884	50863885	G	C	1	GENIC	homozygous	46769696
18	50865135	50865136	C	CTT	1	GENIC	homozygous	46769697
18	50866493	50866494	G	GT	6	GENIC	homozygous	46769701
18	50868171	50868172	G	A	22	GENIC	homozygous	46769703
18	50868360	50868361	A	-	18	GENIC	possibly homozygous	46769704
18	50869578	50869579	G	GC	11	GENIC	heterozygous	46769705
18	50872692	50872693	G	A	1	GENIC	homozygous	46448588