chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	79722247	79722248	G	T	24	GENIC	homozygous	111634545
3	79722609	79722610	T	C	22	GENIC	homozygous	111634546
3	79722943	79722944	T	C	27	GENIC	homozygous	111634547
3	79723589	79723590	C	T	27	GENIC	possibly homozygous	111634550
3	79723772	79723773	C	T	16	GENIC	homozygous	111634551
3	79723815	79723816	C	T	13	GENIC	homozygous	111634552
3	79723822	79723823	A	G	12	GENIC	homozygous	111634553
3	79724310	79724311	A	G	25	GENIC	homozygous	111634554
3	79724560	79724561	G	A	16	GENIC	homozygous	111634555
3	79725012	79725013	G	T	20	GENIC	homozygous	111634556
3	79725305	79725306	T	C	16	GENIC	homozygous	111634557
3	79725928	79725929	C	T	18	GENIC	homozygous	111634559
3	79726852	79726853	A	T	17	GENIC	homozygous	111634560
3	79727459	79727460	T	C	15	GENIC	homozygous	111634561
3	79728178	79728179	C	T	15	GENIC	homozygous	111634562
3	79728716	79728717	A	G	42	GENIC	homozygous	111634563