chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	142087258	142087259	C	G	14	GENIC	homozygous	108937340
1	142088212	142088213	G	A	20	GENIC	homozygous	108937341
1	142089540	142089541	T	C	7	GENIC	homozygous	108937342
1	142089546	142089547	T	C	7	GENIC	homozygous	108937343
1	142091340	142091341	C	T	24	GENIC	homozygous	108937350
1	142091637	142091638	G	A	27	GENIC	possibly homozygous	108937351
1	142092783	142092784	T	C	25	GENIC	homozygous	108937352
1	142095281	142095282	A	G	21	GENIC	homozygous	108262659
1	142096295	142096296	G	C	31	GENIC	homozygous	108937353
1	142097421	142097422	A	G	21	GENIC	homozygous	108937354
1	142097599	142097600	G	A	19	GENIC	homozygous	108937355
1	142097965	142097966	T	G	11	GENIC	homozygous	108937357
1	142098448	142098480	CTTCCTTCCTTCCTTCCTTCCTTCCTTCCTTT		8	GENIC	homozygous	132534361
1	142095748	142095752	CATA		21	GENIC	homozygous	132534356
1	142098049	142098049		GTGTGTGAGTGTGTGTGA	14	GENIC	homozygous	132534358
1	142100490	142100491	A	C	29	GENIC	homozygous	109049770
1	142101150	142101151	T	C	17	GENIC	homozygous	108937359
1	142103044	142103045	A	C	18	GENIC	homozygous	108937360
1	142104770	142104771	T	C	26	GENIC	homozygous	108262665
1	142106434	142106434		A	13	GENIC	homozygous	132534362
1	142106445	142106446	A		14	GENIC	homozygous	132534363
1	142106453	142106453		C	14	GENIC	homozygous	132534364