chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	61813856	61813857	T	C	15	GENIC	homozygous	112670614
4	61814368	61814369	A	C	9	GENIC	homozygous	113028891
4	61814868	61814869	G	A	11	GENIC	homozygous	112670629
4	61814770	61814771	G	A	19	GENIC	homozygous	112670626
4	61815974	61815975	C	G	11	GENIC	heterozygous	126014882
4	61816602	61816603	T	C	20	GENIC	homozygous	112670631
4	61816996	61816997	A	G	20	GENIC	homozygous	126014883
4	61817104	61817105	A	G	11	GENIC	homozygous	126014884
4	61817453	61817454	G	A	13	GENIC	homozygous	126014885
4	61817678	61817679	G	A	21	GENIC	homozygous	126014886
4	61818221	61818222	G	A	10	GENIC	homozygous	126014887
4	61818309	61818310	A	T	16	GENIC	homozygous	126014888
4	61818396	61818397	G	A	19	GENIC	homozygous	126014889
4	61819695	61819696	C	T	31	GENIC	homozygous	126014890
4	61820037	61820038	G	A	28	GENIC	homozygous	126014891
4	61820142	61820143	T	A	18	GENIC	homozygous	126014892
4	61820191	61820192	G	A	19	GENIC	homozygous	126014893
4	61820210	61820211	A	G	17	GENIC	homozygous	126014894
4	61820363	61820364	G	A	8	GENIC	homozygous	126014895
4	61820850	61820851	G	T	12	GENIC	homozygous	126014896
4	61821873	61821874	G	A	20	GENIC	homozygous	126014897
4	61823553	61823554	C	T	20	GENIC	homozygous	126014898
4	61823588	61823589	A	G	20	GENIC	homozygous	126014899
4	61825147	61825148	T	C	16	GENIC	homozygous	126014900
4	61828350	61828351	T	G	14	GENIC	homozygous	126014901
4	61829424	61829425	G	A	5	GENIC	homozygous	126014902
4	61829588	61829589	A	G	11	GENIC	homozygous	126014903
4	61830059	61830060	T	G	26	GENIC	homozygous	126014904
4	61830123	61830124	G	T	26	GENIC	homozygous	126014905