chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	54606126	54606127	G	T	47	GENIC	homozygous	142248176
10	54606150	54606151	A	G	53	GENIC	homozygous	142248177
10	54607018	54607019	T		47	GENIC	possibly homozygous	142203479
10	54607023	54607024	T	C	50	GENIC	possibly homozygous	142248178
10	54607416	54607416		G	56	GENIC	possibly homozygous	142203480
10	54608302	54608318	GTCTGTTCCTCCCAAC		59	GENIC	homozygous	142203481
10	54610003	54610004	G	A	58	GENIC	homozygous	146229844
10	54611799	54611800	A	G	54	GENIC	homozygous	142248179
10	54612246	54612247	G	A	50	GENIC	homozygous	142248180
10	54612718	54612719	C	G	50	GENIC	homozygous	142248181
10	54612872	54612873	A		39	GENIC	homozygous	142203482
10	54613220	54613220		T	47	GENIC	homozygous	142203483
10	54614661	54614661		T	32	GENIC	homozygous	142203484
10	54616200	54616201	A	G	69	GENIC	homozygous	142248182
10	54616367	54616368	A	G	54	GENIC	homozygous	142248183
10	54616993	54616994	T	C	64	GENIC	homozygous	142248184
10	54618504	54618505	T	C	40	GENIC	homozygous	142248185
10	54619077	54619078	G	C	51	GENIC	homozygous	142248186
10	54619204	54619205	C	T	55	GENIC	homozygous	142248187
10	54617134	54617136	AC		44	GENIC	heterozygous	138684716
10	54613121	54613122	C	A	30	GENIC	homozygous	154655127
10	54613120	54613121	C	A	24	GENIC	heterozygous	403634839
10	54613121	54613122	C		30	GENIC	heterozygous	403634840
10	54613120	54613121	C		24	GENIC	possibly homozygous	403634838