chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	110257882	110257883	G	A	16	GENIC	homozygous	114445001
13	110258392	110258393	G	A	43	GENIC	homozygous	114445003
13	110260747	110260748	T	C	21	GENIC	homozygous	114445005
13	110264038	110264039	A	G	19	GENIC	homozygous	114445007
13	110274173	110274174	C	T	21	GENIC	homozygous	114602328
13	110274176	110274177	T	G	23	GENIC	homozygous	114602330
13	110274187	110274188	G	T	22	GENIC	homozygous	114602332
13	110274191	110274192	G	A	23	GENIC	homozygous	114602334
13	110281506	110281507	G	A	30	GENIC	homozygous	114445009
13	110281553	110281554	T	C	23	GENIC	homozygous	114445011
13	110281698	110281699	G	A	25	GENIC	homozygous	114445013
13	110282668	110282669	A	C	29	GENIC	homozygous	114445015
13	110285532	110285533	A	G	21	GENIC	homozygous	114445017
13	110285559	110285560	G	A	22	GENIC	homozygous	114445019
13	110291863	110291864	A	T	21	GENIC	homozygous	114445020
13	110296136	110296137	G	A	23	GENIC	homozygous	114445022
13	110300999	110301000	C	A	15	GENIC	homozygous	114445024
13	110302469	110302470	T	A	21	GENIC	homozygous	114445026
13	110304510	110304511	A	G	17	GENIC	homozygous	114445028
13	110308227	110308228	T	G	21	GENIC	homozygous	114445030