chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	51397255	51397256	G	A	21	GENIC	homozygous	56887321
4	51397430	51397435	ATAAT	-----	2	GENIC	homozygous	58278177
4	51398564	51398565	C	CAT	4	GENIC	homozygous	56887325
4	51405832	51405833	T	TTG	20	GENIC	heterozygous	56887327
4	51405832	51405833	T	TTGTG	20	GENIC	possibly homozygous	56887329
4	51407696	51407697	C	CATAT	3	GENIC	homozygous	56887332
4	51408682	51408683	G	A	47	GENIC	homozygous	56887334
4	51408734	51408735	G	T	58	GENIC	possibly homozygous	56887335
4	51409113	51409114	G	A	32	GENIC	homozygous	56887337
4	51409229	51409230	A	C	24	GENIC	homozygous	56887339
4	51409562	51409563	A	G	15	GENIC	homozygous	56887342
4	51409658	51409659	G	GA	17	GENIC	homozygous	56887343
4	51412871	51412872	A	G	54	GENIC	homozygous	56887345
4	51413206	51413207	T	A	33	GENIC	homozygous	56887347
4	51413966	51413967	T	TA	21	GENIC	possibly homozygous	56887349
4	51414532	51414533	C	T	13	GENIC	homozygous	56887351
4	51414967	51414968	C	T	28	GENIC	homozygous	56887353
4	51415287	51415288	G	A	38	GENIC	homozygous	56887355
4	51415344	51415345	G	A	19	GENIC	homozygous	56887357
4	51415829	51415830	T	C	39	GENIC	homozygous	56887359
4	51416237	51416238	T	TACCG	20	GENIC	homozygous	56887361
4	51417013	51417017	TGTG	----	20	GENIC	heterozygous	56887363
4	51417015	51417017	TG	--	20	GENIC	heterozygous	56887365
4	51417234	51417235	G	A	29	GENIC	homozygous	56887367
4	51403124	51403125	C	A	14	GENIC	homozygous	58333851