chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	15562167	15562168	T	C	12	GENIC	homozygous	111454865
3	15562285	15562286	T	C	19	GENIC	homozygous	119697567
3	15562348	15562349	A	G	17	GENIC	homozygous	111454868
3	15562923	15562924	C	T	14	GENIC	possibly homozygous	119697568
3	15562958	15562959	A	G	13	GENIC	homozygous	111454871
3	15567412	15567413	T	G	29	GENIC	homozygous	119697569
3	15567586	15567587	C	T	18	GENIC	homozygous	119697570
3	15569198	15569199	A	G	24	GENIC	homozygous	111454887
3	15569328	15569329	G	A	24	GENIC	homozygous	119697571
3	15570853	15570854	C	T	23	GENIC	homozygous	119697572
3	15571734	15571735	C	T	11	GENIC	homozygous	119697573
3	15572578	15572579	C	T	8	GENIC	homozygous	119697574
3	15576942	15576943	T	G	25	GENIC	homozygous	119697575
3	15577248	15577249	C	T	31	GENIC	homozygous	119697576
3	15579321	15579322	T	C	25	GENIC	homozygous	119697577
3	15581045	15581046	G	T	21	GENIC	homozygous	111454911
3	15581609	15581610	A	T	25	GENIC	homozygous	119697578
3	15581802	15581803	C	G	15	GENIC	homozygous	119697579
3	15582197	15582198	T	C	20	GENIC	homozygous	119697580
3	15582315	15582316	G	A	15	GENIC	homozygous	119697581