chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	109297919	109297920	T	A	26	GENIC	homozygous	57589582
3	109297975	109297976	T	C	27	GENIC	homozygous	57589585
3	109297991	109297992	T	C	25	GENIC	homozygous	57589587
3	109298241	109298242	G	GTT	20	GENIC	possibly homozygous	57589590
3	109298241	109298242	G	GTTTTT	20	GENIC	heterozygous	57976983
3	109299190	109299191	A	T	19	GENIC	homozygous	57589604
3	109299363	109299364	C	T	23	GENIC	homozygous	57589606
3	109299377	109299378	G	C	16	GENIC	homozygous	57589608
3	109299633	109299634	C	CAGTGA	13	GENIC	homozygous	57589611
3	109299665	109299666	A	C	18	GENIC	homozygous	57589613
3	109300312	109300313	C	A	35	GENIC	homozygous	57589618