chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	157464291	157464292	C	T	57	GENIC	homozygous	109154225
1	157464806	157464807	A	G	29	GENIC	homozygous	109154227
1	157464909	157464910	A	T	42	GENIC	possibly homozygous	109154229
1	157466126	157466127	C	T	43	GENIC	possibly homozygous	109154231
1	157468241	157468242	T	C	32	GENIC	homozygous	108325728
1	157468748	157468749	T	C	48	GENIC	homozygous	109154233
1	157470447	157470448	C	T	44	GENIC	homozygous	109154235
1	157471671	157471672	A	C	32	GENIC	homozygous	108325730
1	157473671	157473672	G	T	49	GENIC	homozygous	108325732
1	157474675	157474676	C	T	26	GENIC	homozygous	109154237
1	157475917	157475918	C	T	62	GENIC	homozygous	109154239
1	157476224	157476225	C	T	61	GENIC	homozygous	109154241
1	157476752	157476753	T	C	38	GENIC	possibly homozygous	109154243
1	157478188	157478189	A	C	48	GENIC	homozygous	109154245
1	157479204	157479205	A	G	43	GENIC	possibly homozygous	109154247
1	157479392	157479393	G	A	59	GENIC	homozygous	109154249
1	157483555	157483556	C	T	34	GENIC	heterozygous	109154251
1	157487440	157487441	T	G	45	GENIC	possibly homozygous	109154253
1	157488567	157488568	G	A	55	GENIC	homozygous	109154255
1	157490939	157490940	A	G	46	GENIC	homozygous	109154257
1	157491443	157491444	C	T	59	GENIC	possibly homozygous	109154259
1	157491880	157491881	T	C	73	GENIC	homozygous	109154261