chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	166739132	166739133	T	C	31	GENIC	homozygous	57770390
3	166739436	166739437	G	A	33	GENIC	homozygous	57770391
3	166739575	166739576	C	A	23	GENIC	homozygous	57770392
3	166739771	166739772	C	G	29	GENIC	homozygous	57770393
3	166740357	166740358	T	C	28	GENIC	homozygous	57770394
3	166740709	166740710	A	G	29	GENIC	homozygous	57770395
3	166741254	166741255	C	T	36	GENIC	homozygous	57770396
3	166741838	166741839	C	G	31	GENIC	homozygous	57770397
3	166741865	166741866	A	G	30	GENIC	homozygous	57770398
3	166742009	166742010	A	G	11	GENIC	homozygous	57770399
3	166742318	166742319	G	GTATTTATT	3	GENIC	homozygous	58631045
3	166742366	166742367	T	TTTCTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTACGTTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACTCCTTTATTTTATTTATTTATTTATTTTTTTGG	7	GENIC	homozygous	58631046
3	166742474	166742475	A	AT	9	GENIC	homozygous	57770406
3	166742504	166742505	T	C	15	GENIC	homozygous	57770408
3	166742720	166742721	A	ATT	9	GENIC	homozygous	57770410
3	166742740	166742743	TTT	---	11	GENIC	homozygous	57770411
3	166742933	166742934	T	C	19	GENIC	possibly homozygous	57770412
3	166743473	166743474	G	A	6	GENIC	homozygous	57770413
3	166744739	166744740	C	CCTAT	12	GENIC	homozygous	57770414
3	166745488	166745489	T	C	32	GENIC	homozygous	57770415