chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	57584130	57584131	C	T	8	GENIC	homozygous	142251127
10	57585262	57585263	G	T	11	GENIC	homozygous	142251128
10	57587053	57587054	G	A	8	GENIC	homozygous	142251129
10	57587407	57587408	G	C	10	GENIC	homozygous	142251130
10	57587605	57587606	T	C	12	GENIC	homozygous	142251131
10	57588092	57588093	A	T	18	GENIC	homozygous	142251132
10	57589237	57589238	G	A	11	GENIC	homozygous	142251133
10	57589444	57589445	G	A	16	GENIC	homozygous	142251134
10	57590003	57590004	T	C	21	GENIC	homozygous	142251135
10	57590073	57590074	T	G	10	GENIC	homozygous	142251136
10	57591097	57591098	C	G	13	GENIC	homozygous	142251137
10	57591154	57591155	C	A	12	GENIC	homozygous	138796462
10	57594489	57594490	G	A	11	GENIC	homozygous	142251138
10	57597098	57597098		G	9	GENIC	heterozygous	138685367
10	57597820	57597821	T	C	19	GENIC	homozygous	138796475
10	57601819	57601820	G	A	20	GENIC	homozygous	142251139
10	57602465	57602466	A	C	22	GENIC	homozygous	138796481
10	57602783	57602784	G	A	20	GENIC	homozygous	142251140
10	57603253	57603254	T	A	20	GENIC	homozygous	142251141
10	57604503	57604504	C	T	13	GENIC	homozygous	142251142
10	57604604	57604605	G	A	15	GENIC	homozygous	142251143
10	57604789	57604789		TGTGTCTATCTCTG	12	GENIC	homozygous	138685368
10	57606398	57606399	T	G	12	GENIC	homozygous	138796489
10	57608960	57608960		A	12	GENIC	homozygous	138685370
10	57609368	57609369	A	G	16	GENIC	homozygous	138796492
10	57610643	57610644	A	G	17	GENIC	homozygous	138796495
10	57601553	57601556	CTC		14	GENIC	homozygous	142204180
10	57601701	57601701		TG	10	GENIC	possibly homozygous	142204181
10	57605992	57605994	TG		11	GENIC	homozygous	142204182