chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	56068881	56068882	A	G	14	GENIC	homozygous	137474821
5	56068919	56068921	GG		11	GENIC	homozygous	137309704
5	56069015	56069016	C	T	12	GENIC	homozygous	137474822
5	56069313	56069314	G	T	20	GENIC	homozygous	137474823
5	56069445	56069445		A	10	GENIC	homozygous	137309705
5	56069468	56069469	C	T	13	GENIC	homozygous	137474824
5	56069505	56069506	G	A	17	GENIC	homozygous	137474825
5	56069825	56069826	T	A	13	GENIC	possibly homozygous	137474826
5	56070156	56070157	T		15	GENIC	homozygous	137309706
5	56070941	56070942	G	A	22	GENIC	homozygous	137474827
5	56071353	56071354	T	C	20	GENIC	homozygous	137474828
5	56071694	56071695	C	A	25	GENIC	homozygous	137474829
5	56071756	56071757	T	C	25	GENIC	homozygous	137474830
5	56072137	56072138	C	T	18	GENIC	homozygous	137474831
5	56072450	56072451	T	C	11	GENIC	homozygous	137474832
5	56072670	56072671	C	G	22	GENIC	homozygous	137474833
5	56072776	56072777	G	A	23	GENIC	homozygous	137474834
5	56072818	56072819	T	C	19	GENIC	homozygous	137474835
5	56073435	56073436	A	G	16	GENIC	homozygous	137474836
5	56073693	56073694	C	T	18	GENIC	homozygous	137474837
5	56073882	56073883	C	T	34	GENIC	homozygous	137474838
5	56076561	56076562	T	C	24	GENIC	homozygous	137474839