chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	54606126	54606127	G	T	30	GENIC	homozygous	142248176
10	54606150	54606151	A	G	25	GENIC	homozygous	142248177
10	54607018	54607019	T		19	GENIC	homozygous	142203479
10	54607023	54607024	T	C	19	GENIC	homozygous	142248178
10	54607416	54607416		G	24	GENIC	homozygous	142203480
10	54611799	54611800	A	G	39	GENIC	homozygous	142248179
10	54612246	54612247	G	A	22	GENIC	homozygous	142248180
10	54612718	54612719	C	G	28	GENIC	homozygous	142248181
10	54614661	54614661		T	18	GENIC	homozygous	142203484
10	54608302	54608318	GTCTGTTCCTCCCAAC		37	GENIC	homozygous	142203481
10	54612872	54612873	A		22	GENIC	homozygous	142203482
10	54613220	54613220		T	25	GENIC	homozygous	142203483
10	54613121	54613122	C	A	28	GENIC	homozygous	154655127
10	54614572	54614573	T	A	17	GENIC	homozygous	154655128
10	54613120	54613121	C		27	GENIC	possibly homozygous	403634838
10	54613120	54613121	C	A	27	GENIC	heterozygous	403634839
10	54613121	54613122	C		28	GENIC	heterozygous	403634840
10	54616200	54616201	A	G	38	GENIC	homozygous	142248182
10	54616367	54616368	A	G	21	GENIC	homozygous	142248183
10	54616993	54616994	T	C	37	GENIC	homozygous	142248184
10	54617134	54617136	AC		26	GENIC	heterozygous	138684716
10	54618504	54618505	T	C	18	GENIC	homozygous	142248185
10	54619077	54619078	G	C	16	GENIC	homozygous	142248186
10	54619204	54619205	C	T	19	GENIC	homozygous	142248187
10	54618132	54618132		AT	22	GENIC	homozygous	145729696
10	54615621	54615624	GTC		23	GENIC	homozygous	145729695