chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	54606126	54606127	G	T	12	GENIC	homozygous	142248176
10	54606150	54606151	A	G	15	GENIC	homozygous	142248177
10	54607018	54607019	T		11	GENIC	homozygous	142203479
10	54607023	54607024	T	C	12	GENIC	homozygous	142248178
10	54607416	54607416		G	19	GENIC	homozygous	142203480
10	54608302	54608318	GTCTGTTCCTCCCAAC		15	GENIC	homozygous	142203481
10	54611799	54611800	A	G	15	GENIC	homozygous	142248179
10	54612246	54612247	G	A	21	GENIC	homozygous	142248180
10	54612718	54612719	C	G	11	GENIC	homozygous	142248181
10	54612872	54612873	A		11	GENIC	homozygous	142203482
10	54613220	54613220		T	8	GENIC	homozygous	142203483
10	54614661	54614661		T	15	GENIC	homozygous	142203484
10	54618504	54618505	T	C	13	GENIC	homozygous	142248185
10	54613121	54613122	C	A	8	GENIC	homozygous	154655127
10	54616200	54616201	A	G	15	GENIC	homozygous	142248182
10	54616367	54616368	A	G	10	GENIC	homozygous	142248183
10	54616993	54616994	T	C	11	GENIC	homozygous	142248184
10	54613120	54613121	C		8	GENIC	homozygous	403634838
10	54613120	54613121	C	A	8	GENIC	heterozygous	403634839
10	54613121	54613122	C		8	GENIC	heterozygous	403634840
10	54619077	54619078	G	C	10	GENIC	homozygous	142248186
10	54619204	54619205	C	T	10	GENIC	homozygous	142248187