chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	79722247	79722248	G	T	46	GENIC	homozygous	111634545
3	79722609	79722610	T	C	50	GENIC	homozygous	111634546
3	79722943	79722944	T	C	54	GENIC	homozygous	111634547
3	79723148	79723148		TTTTTTTT	28	GENIC	homozygous	127900123
3	79723152	79723152		TT	28	GENIC	homozygous	127900124
3	79723164	79723165	T	C	37	GENIC	homozygous	111634548
3	79723589	79723590	C	T	39	GENIC	homozygous	111634550
3	79723772	79723773	C	T	51	GENIC	homozygous	111634551
3	79723815	79723816	C	T	54	GENIC	homozygous	111634552
3	79723822	79723823	A	G	52	GENIC	homozygous	111634553
3	79724310	79724311	A	G	61	GENIC	homozygous	111634554
3	79724560	79724561	G	A	61	GENIC	homozygous	111634555
3	79724986	79724986		GAGATTTTGTTAAAAACAAA	59	GENIC	homozygous	127900125
3	79725012	79725013	G	T	61	GENIC	possibly homozygous	111634556
3	79725305	79725306	T	C	72	GENIC	homozygous	111634557
3	79725914	79725916	AC		21	GENIC	homozygous	127900126
3	79725923	79725924	C	T	17	GENIC	homozygous	111634558
3	79725928	79725929	C	T	20	GENIC	homozygous	111634559
3	79726852	79726853	A	T	45	GENIC	homozygous	111634560
3	79727459	79727460	T	C	57	GENIC	homozygous	111634561
3	79728166	79728168	TT		55	GENIC	homozygous	127900127
3	79728178	79728179	C	T	57	GENIC	homozygous	111634562
3	79728716	79728717	A	G	63	GENIC	homozygous	111634563