chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	51397255	51397256	G	A	17	GENIC	homozygous	56887321
4	51408682	51408683	G	A	23	GENIC	possibly homozygous	56887334
4	51408734	51408735	G	T	26	GENIC	possibly homozygous	56887335
4	51409113	51409114	G	A	18	GENIC	homozygous	56887337
4	51409229	51409230	A	C	25	GENIC	homozygous	56887339
4	51412871	51412872	A	G	19	GENIC	possibly homozygous	56887345
4	51413206	51413207	T	A	8	GENIC	possibly homozygous	56887347
4	51413966	51413967	T	TA	3	GENIC	heterozygous	56887349
4	51414532	51414533	C	T	11	GENIC	homozygous	56887351
4	51414967	51414968	C	T	16	GENIC	possibly homozygous	56887353
4	51415287	51415288	G	A	16	GENIC	possibly homozygous	56887355
4	51415344	51415345	G	A	9	GENIC	homozygous	56887357
4	51415829	51415830	T	C	28	GENIC	possibly homozygous	56887359
4	51416237	51416238	T	TACCG	4	GENIC	homozygous	56887361
4	51417015	51417017	TG	--	1	GENIC	homozygous	56887365
4	51417234	51417235	G	A	20	GENIC	possibly homozygous	56887367