chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	24089505	24089506	A	G	35	GENIC	homozygous	60639373
1	24089568	24089569	T	C	27	GENIC	homozygous	60639374
1	24091221	24091222	G	C	34	GENIC	homozygous	60639375
1	24092442	24092443	G	A	43	GENIC	homozygous	60639377
1	24095968	24095969	C	A	30	GENIC	homozygous	60639378
1	24096487	24096488	G	C	23	GENIC	homozygous	60639379
1	24096664	24096665	T	G	28	GENIC	homozygous	60639380
1	24096800	24096801	A	G	27	GENIC	homozygous	60639381
1	24096979	24096980	A	G	36	GENIC	homozygous	60639382
1	24097287	24097288	A	C	27	GENIC	homozygous	60639383
1	24097754	24097755	C	-	20	GENIC	homozygous	60639384
1	24097984	24097985	C	T	26	GENIC	homozygous	60639385
1	24098008	24098009	A	C	27	GENIC	homozygous	60639386
1	24098420	24098421	T	C	38	GENIC	homozygous	60639387
1	24098642	24098643	G	C	28	GENIC	homozygous	60639388
1	24098963	24098964	C	G	25	GENIC	homozygous	60639389
1	24098964	24098965	A	G	27	GENIC	homozygous	60639390
1	24098974	24098975	A	T	29	GENIC	homozygous	60639391
1	24098975	24098976	A	G	29	GENIC	homozygous	60639392
1	24098980	24098983	GAC	---	30	GENIC	homozygous	62072829
1	24098984	24098985	A	ATTT	29	GENIC	homozygous	62363661
1	24098985	24098986	G	T	29	GENIC	homozygous	62363662
1	24099590	24099591	T	TA	10	GENIC	possibly homozygous	60639393