chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	172380101	172380102	G	T	23	GENIC	homozygous	111837338
3	172384401	172384402	C	A	42	GENIC	homozygous	111837340
3	172398901	172398902	G	T	25	GENIC	homozygous	111837342
3	172400989	172400990	C	T	7	GENIC	homozygous	111837344
3	172417643	172417644	T	C	49	GENIC	homozygous	111837346
3	172419537	172419538	C	T	11	GENIC	homozygous	111837348
3	172419542	172419543	G	T	14	GENIC	possibly homozygous	111837350
3	172419552	172419553	T	C	15	GENIC	homozygous	111837352
3	172419623	172419624	T	G	23	GENIC	homozygous	111837354
3	172419672	172419673	T	G	26	GENIC	homozygous	111837356
3	172420738	172420739	C	G	11	GENIC	homozygous	111837358
3	172420782	172420783	G	C	6	GENIC	homozygous	111837360
3	172421083	172421084	C	G	24	GENIC	homozygous	111837362
3	172423265	172423266	T	G	42	GENIC	heterozygous	111837364
3	172430163	172430164	G	C	47	GENIC	homozygous	111837366
3	172433034	172433035	G	A	34	GENIC	possibly homozygous	111837368
3	172433053	172433054	G	T	35	GENIC	homozygous	111837370
3	172433615	172433616	A	T	50	GENIC	possibly homozygous	111837372