chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	103303487	103303488	C	A	22	GENIC	possibly homozygous	138400740
8	103304227	103304228	A	C	22	GENIC	homozygous	138400743
8	103304485	103304486	C	T	13	GENIC	homozygous	138400745
8	103305007	103305008	T	C	13	GENIC	homozygous	138400746
8	103305305	103305306	C	T	19	GENIC	homozygous	138400747
8	103305440	103305441	C	T	26	GENIC	homozygous	146217053
8	103305584	103305585	G	A	23	GENIC	homozygous	146217054
8	103306218	103306219	C	G	14	GENIC	homozygous	146217055
8	103306878	103306879	T	C	23	GENIC	homozygous	142094505
8	103307292	103307293	T	C	23	GENIC	homozygous	146217056
8	103307579	103307580	G	T	16	GENIC	homozygous	142094509
8	103307583	103307584	G	T	17	GENIC	homozygous	142094510
8	103307883	103307884	A	G	11	GENIC	homozygous	142094512
8	103307958	103307959	T	C	13	GENIC	homozygous	142094513
8	103308419	103308420	G	A	32	GENIC	homozygous	146217057
8	103308875	103308876	T	G	34	GENIC	homozygous	142094516
8	103308983	103308984	G	A	26	GENIC	homozygous	146217058
8	103309041	103309042	T	A	21	GENIC	homozygous	142094517
8	103309415	103309416	C	T	18	GENIC	homozygous	146217059
8	103310103	103310104	A	G	20	GENIC	homozygous	142094519
8	103310481	103310482	G	A	22	GENIC	homozygous	146217060
8	103311033	103311034	G	A	21	GENIC	homozygous	146217061
8	103311543	103311544	G	T	25	GENIC	homozygous	142094521
8	103312062	103312063	A	G	20	GENIC	homozygous	142094522
8	103312614	103312615	T	C	19	GENIC	homozygous	142094523
8	103312803	103312804	T	C	24	GENIC	homozygous	142094524
8	103312879	103312880	T	G	21	GENIC	homozygous	142094525
8	103315398	103315399	C	T	12	GENIC	homozygous	142094527
8	103315748	103315749	T	C	25	GENIC	homozygous	146217062
8	103314727	103314727		C	18	GENIC	homozygous	138261308
8	103306903	103307005	AATCTACTCTCTTTTTTTTTTTTCCTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAACCCC		21	GENIC	homozygous	142029201
8	103308599	103308609	TGGGGGGGGG		9	GENIC	homozygous	142029202